Allele Registry

Canonical Allele Identifier: PA2826464714

Gene: MSH2 HGNC NCBI

ClinVar RCV:

RCV000121563

RCV000543103

RCV001804848

RCV003325461

RCV004530024

ClinVar Variation:

134844

HGVS (amino-acid)	Matching Registered Transcripts
NP_001245210.1:p.Ala534Ser	CA019328 NM_001258281.1:c.1600G>T