Allele Registry

Canonical Allele Identifier: PA2826463298

Gene: MSH2 HGNC NCBI

Linked Data - NCBI & NCI

ClinVar Allele:

150524

ClinVar RCV:

RCV000128997

RCV000228319

RCV000235651

RCV000759122

RCV001269353

RCV003333736

RCV003997470

RCV004532540

ClinVar Variation:

140810

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001245210.1:p.Pro193Ser	CA022230 NM_001258281.1:c.577C>T