Allele Registry

Canonical Allele Identifier: PA331604

Gene: MSH2 HGNC NCBI

MaveDb:

Score 2.9635800281

ClinVar Allele:

96586

ClinVar RCV:

RCV000076614

RCV000630010

RCV003584547

ClinVar Variation:

91111

HGVS (amino-acid)	Matching Registered Transcripts
NP_000242.1:p.Tyr165Asp	CA021222 NM_000251.3:c.493T>G