Canonical Allele Identifier: PA2826465585
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 141351
ClinVar RCV Id: RCV000129838 RCV000168339 RCV000482932 RCV003335115 RCV003997529 RCV004532554
ClinVar Variation Id: 631127
ClinVar RCV Id: RCV000777250 RCV000807280 RCV001175571 RCV001356219 RCV003336181
ClinVar Variation Id: 1047398
ClinVar RCV Id: RCV001352102
JSON-LD

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