Canonical Allele Identifier: PA2826626076
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1775540
ClinVar RCV Id: RCV002392620
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Ser395Arg
CA346746803
NM_001281492.2:c.1183A>C
CA346746821
NM_001281492.2:c.1185T>A
CA346746822
NM_001281492.2:c.1185T>G