Allele Registry

Canonical Allele Identifier: PA658671778

Gene: MSH2 HGNC NCBI

ClinVar RCV:

RCV000526049

RCV000579804

RCV001584241

RCV004003753

ClinVar Variation:

455601

HGVS (amino-acid)	Matching Registered Transcripts
NP_000242.1:p.Glu205Gln	CA46678574 NM_000251.3:c.613G>C