Allele Registry

Canonical Allele Identifier: PA294301

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000131160

RCV000212679

RCV001083021

RCV001137558

RCV003153343

RCV004537277

ClinVar Variation:

89359

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.Pro1087Thr	CA012215 NM_000179.3:c.3259C>A