Allele Registry

Canonical Allele Identifier: PA658804046

Gene: MSH2 HGNC NCBI

ClinVar RCV:

RCV000629723

RCV001013211

RCV001731820

RCV004002772

ClinVar Variation:

525615

HGVS (amino-acid)	Matching Registered Transcripts
NP_000242.1:p.Ala604Thr	CA346728336 NM_000251.3:c.1810G>A