Allele Registry

Canonical Allele Identifier: PA2826464720

Gene: MSH2 HGNC NCBI

ClinVar RCV:

RCV000574655

RCV000584510

RCV000735960

RCV000796750

ClinVar Variation:

479829

491787

HGVS (amino-acid)	Matching Registered Transcripts
NP_001245210.1:p.Gln535His	CA346728326 NM_001258281.1:c.1605G>C CA346728327 NM_001258281.1:c.1605G>T