Canonical Allele Identifier: PA2826630993
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1783448
ClinVar RCV Id: RCV002421757
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Met352Lys
CA346750582
NM_001281493.2:c.1055T>A