Canonical Allele Identifier: PA2826635612
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 2817259
ClinVar RCV Id: RCV003760929
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Gly372Ala
CA346750703
NM_001281494.2:c.1115G>C