Allele Registry

Canonical Allele Identifier: PA645378206

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000480607

RCV000823347

RCV002329143

RCV004002284

ClinVar Variation:

419079

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.Gly39Ala	CA067248 NM_000179.3:c.116G>C