Allele Registry

Canonical Allele Identifier: PA645383821

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000230242

RCV000487138

RCV000570386

RCV003998729

ClinVar Variation:

237188

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.Cys1117Phe	CA070699 NM_000179.3:c.3350G>T