Allele Registry

Canonical Allele Identifier: PA168316

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000131534

RCV000202300

RCV002510780

RCV002513797

RCV003450969

RCV004555853

ClinVar Variation:

89393

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.Gly1157Ser	CA012971 NM_000179.3:c.3469G>A