Canonical Allele Identifier: PA2826626799
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 455175
ClinVar RCV Id: RCV000536294 RCV000776692 RCV004003670
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Cys557Ser
CA346750771
NM_001281492.2:c.1669T>A
CA346750775
NM_001281492.2:c.1670G>C