Allele Registry

Canonical Allele Identifier: PA658671483

Gene: MSH2 HGNC NCBI

ClinVar RCV:

RCV000560975

RCV001867892

RCV003447542

ClinVar Variation:

483666

HGVS (amino-acid)	Matching Registered Transcripts
NP_000242.1:p.Ala54Val	CA029814 NM_000251.3:c.161C>T