Allele Registry

Canonical Allele Identifier: PA645384339

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000491433

RCV002523978

RCV003449281

RCV004003451

ClinVar Variation:

428285

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.Leu1209Pro	CA346760597 NM_000179.3:c.3626T>C