Allele Registry

Canonical Allele Identifier: PA287456

Gene: MSH2 HGNC NCBI

ClinVar RCV:

RCV000030254

RCV000115531

RCV000212584

RCV001079015

ClinVar Variation:

36578

HGVS (amino-acid)	Matching Registered Transcripts
NP_000242.1:p.Met141Val	CA021148 NM_000251.3:c.421A>G