Allele Registry

Canonical Allele Identifier: PA331470

Gene: MSH2 HGNC NCBI

ClinVar RCV:

RCV000535935

RCV000574384

RCV003997159

RCV004537294

ClinVar Variation:

90907

HGVS (amino-acid)	Matching Registered Transcripts
NP_000242.1:p.Ala714Val	CA020132 NM_000251.3:c.2141C>T