Allele Registry

Canonical Allele Identifier: PA331503

Gene: MSH2 HGNC NCBI

ClinVar RCV:

RCV000491833

RCV000684788

ClinVar Variation:

90950

HGVS (amino-acid)	Matching Registered Transcripts
NP_000242.1:p.Trp764Cys	CA020440 NM_000251.3:c.2292G>C CA346729840 NM_000251.3:c.2292G>T