Allele Registry

Canonical Allele Identifier: PA357582

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000205525

RCV000214718

RCV000985830

RCV002254688

RCV003993891

RCV003997625

ClinVar Variation:

220238

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.Thr719Ile	CA068506 NM_000179.3:c.2156C>T