Allele Registry

Canonical Allele Identifier: PA2826626489

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000630018

ClinVar Variation:

525753

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268421.1:p.Leu487Arg	CA346749734 NM_001281492.2:c.1460T>G