Allele Registry

Canonical Allele Identifier: PA2825088584

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV003595096

ClinVar Variation:

2710370

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.Gly571Arg	CA068053 NM_000179.3:c.1711G>C