Allele Registry

Canonical Allele Identifier: PA658672732

Gene: MSH2 HGNC NCBI

MaveDb:

Score -4.0251341115

ClinVar RCV:

RCV000574655

RCV000584510

RCV000735960

RCV000796750

ClinVar Variation:

479829

491787

HGVS (amino-acid)	Matching Registered Transcripts
NP_000242.1:p.Gln601His	CA346728326 NM_000251.3:c.1803G>C CA346728327 NM_000251.3:c.1803G>T