Allele Registry

Canonical Allele Identifier: PA645471562

Gene: MSH2 HGNC NCBI

ClinVar RCV:

RCV000759834

RCV000773079

RCV001246708

RCV003470539

RCV004002296

ClinVar Variation:

419266

HGVS (amino-acid)	Matching Registered Transcripts
NP_000242.1:p.Met141Thr	CA038657 NM_000251.3:c.422T>C