Canonical Allele Identifier: PA2826624751
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1773762
ClinVar RCV Id: RCV002389679
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Trp50Gly
CA346734932
NM_001281492.2:c.148T>G