Allele Registry

Canonical Allele Identifier: PA095134

Gene: MSH2 HGNC NCBI

ClinVar RCV:

RCV000213657

RCV002514351

RCV003452845

ClinVar Variation:

90715

HGVS (amino-acid)	Matching Registered Transcripts
NP_000242.1:p.Thr552Pro	CA018802 NM_000251.3:c.1654A>C