Canonical Allele Identifier: PA916010910
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 455305
ClinVar RCV Id: RCV000525094 RCV000567533
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Lys13Met
CA346734528
NM_001281492.2:c.38A>T