Allele Registry

Canonical Allele Identifier: PA645474982

Gene: MSH2 HGNC NCBI

ClinVar RCV:

RCV000220154

RCV001220357

RCV002247660

RCV003997980

ClinVar Variation:

232518

HGVS (amino-acid)	Matching Registered Transcripts
NP_000242.1:p.Ala649Val	CA10577989 NM_000251.3:c.1946C>T