Allele Registry

Canonical Allele Identifier: PA2573165019

Gene: MSH2 HGNC NCBI

ClinVar RCV:

RCV001960257

ClinVar Variation:

1442394

HGVS (amino-acid)	Matching Registered Transcripts
NP_000242.1:p.Leu93Val	CA346729584 NM_000251.3:c.277C>G