Allele Registry

Canonical Allele Identifier: PA2826465813

Gene: MSH2 HGNC NCBI

Linked Data - NCBI & NCI

ClinVar Allele:

180031

ClinVar RCV:

RCV000203841

RCV000565478

RCV000708846

RCV000759828

RCV001193897

RCV001354344

RCV003467250

ClinVar Variation:

182587

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001245210.1:p.Ala803Glu	CA020801 NM_001258281.1:c.2408C>A