Allele Registry

Canonical Allele Identifier: PA167742

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000131189

RCV000485534

RCV000524119

RCV001818236

RCV002498356

RCV003466936

RCV004019093

ClinVar Variation:

89219

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.Ser580Leu	CA009108 NM_000179.3:c.1739C>T