Allele Registry

Canonical Allele Identifier: PA299335

Gene: MSH2 HGNC NCBI

Linked Data

ClinVar RCV:

RCV000160599

RCV000219973

RCV000813805

RCV000814388

RCV002422813

RCV003324799

RCV004001761

ClinVar Variation:

182569

657719

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_000242.1:p.Gln681His	CA019887 NM_000251.3:c.2043A>T CA033402 NM_000251.3:c.2043A>C