Canonical Allele Identifier: PA2826627145
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 2502856
ClinVar RCV Id: RCV003229514

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Gly640Cys
CA346753105
NM_001281492.2:c.1918G>T