Allele Registry

Canonical Allele Identifier: PA916011932

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000131534

RCV000202300

RCV002510780

RCV002513797

RCV003450969

RCV004555853

ClinVar Variation:

89393

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268423.1:p.Gly855Ser	CA012971 NM_001281494.2:c.2563G>A