Allele Registry

Canonical Allele Identifier: PA165541

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000130018

RCV000410453

RCV000804545

RCV003997541

ClinVar Variation:

141475

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.Glu226Gly	CA016211 NM_000179.3:c.677A>G