Allele Registry

Canonical Allele Identifier: PA2826464339

Gene: MSH2 HGNC NCBI

Linked Data

ClinVar RCV:

RCV000131303

RCV000160591

RCV000235175

RCV000548522

RCV000823121

RCV001137232

RCV003315905

RCV003998473

RCV004544469

ClinVar Variation:

142279

182563

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001245210.1:p.Gln444His	CA018560 NM_001258281.1:c.1332G>C CA018566 NM_001258281.1:c.1332G>T