Allele Registry

Canonical Allele Identifier: PA645474657

Gene: MSH2 HGNC NCBI

ClinVar RCV:

RCV000484349

RCV000581019

RCV000630236

RCV004003366

ClinVar Variation:

421910

HGVS (amino-acid)	Matching Registered Transcripts
NP_000242.1:p.Ile577Val	CA030657 NM_000251.3:c.1729A>G