Allele Registry

Canonical Allele Identifier: PA658680861

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000564228

RCV000688061

RCV000765685

RCV001591322

RCV003470823

RCV004000868

ClinVar Variation:

479867

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.Lys728Arg	CA068575 NM_000179.3:c.2183A>G