Allele Registry

Canonical Allele Identifier: PA287454

Gene: MSH2 HGNC NCBI

ClinVar RCV:

RCV000115530

RCV000199902

RCV000217044

RCV000411543

RCV001175574

RCV003997279

ClinVar Variation:

127646

HGVS (amino-acid)	Matching Registered Transcripts
NP_000242.1:p.Leu135Phe	CA021136 NM_000251.3:c.403C>T