Allele Registry

Canonical Allele Identifier: PA192416

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000165060

RCV000201982

RCV000410385

RCV000656900

RCV001082754

RCV003323297

ClinVar Variation:

185611

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.Val1160Ile	CA013029 NM_000179.3:c.3478G>A