Allele Registry

Canonical Allele Identifier: PA658743735

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000581415

ClinVar Variation:

491868

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.Gly39Val	CA346734861 NM_000179.3:c.116G>T