Allele Registry

Canonical Allele Identifier: PA2826465154

Gene: MSH2 HGNC NCBI

ClinVar Allele:

232619

ClinVar RCV:

RCV000215093

RCV003454614

ClinVar Variation:

229885

HGVS (amino-acid)	Matching Registered Transcripts
NP_001245210.1:p.Ala634Glu	CA10577997 NM_001258281.1:c.1901C>A