Canonical Allele Identifier: PA916012267
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 824242
ClinVar RCV Id: RCV001021196 RCV001861011
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Cys967Tyr
CA346761219
NM_001281494.2:c.2900G>A