Allele Registry

Canonical Allele Identifier: PA915984303

Gene: MSH2 HGNC NCBI

ClinVar RCV:

RCV000588121

RCV004002417

ClinVar Variation:

495771

HGVS (amino-acid)	Matching Registered Transcripts
NP_001245210.1:p.Gln94Lys	CA346730592 NM_001258281.1:c.280C>A