Allele Registry

Canonical Allele Identifier: PA331529

Gene: MSH2 HGNC NCBI

ClinVar RCV:

RCV000662430

RCV000692140

RCV000774582

RCV001818241

ClinVar Variation:

91003

HGVS (amino-acid)	Matching Registered Transcripts
NP_000242.1:p.Tyr856Cys	CA020747 NM_000251.3:c.2567A>G