Canonical Allele Identifier: PA2826625135
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 187031
ClinVar RCV Id: RCV000166713 RCV000800357
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Arg170Leu
CA016620
NM_001281492.2:c.509G>T