Allele Registry

Canonical Allele Identifier: PA915984021

Gene: MSH2 HGNC NCBI

ClinVar RCV:

RCV000465504

RCV000774555

RCV003129863

RCV004000782

ClinVar Variation:

408502

HGVS (amino-acid)	Matching Registered Transcripts
NP_001245210.1:p.Asn43Ser	CA037887 NM_001258281.1:c.128A>G