Allele Registry

Canonical Allele Identifier: PA2826465585

Gene: MSH2 HGNC NCBI

Linked Data - NCBI & NCI

ClinVar Allele:

151065

616656

1024553

ClinVar RCV:

RCV000129838

RCV000168339

RCV000482932

RCV000777250

RCV000807280

RCV001175571

RCV001352102

RCV001356219

RCV003335115

RCV003336181

RCV003997529

RCV004532554

ClinVar Variation:

141351

631127

1047398

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001245210.1:p.Met747Ile	CA020596 NM_001258281.1:c.2241G>A CA46705323 NM_001258281.1:c.2241G>C CA346730278 NM_001258281.1:c.2241G>T