Allele Registry

Canonical Allele Identifier: PA1139676105

Gene: MSH2 HGNC NCBI

ClinVar RCV:

RCV001190993

RCV003770150

ClinVar Variation:

927599

HGVS (amino-acid)	Matching Registered Transcripts
NP_000242.1:p.Ala15Val	CA346728545 NM_000251.3:c.44C>T