Canonical Allele Identifier: PA2573192025
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1517490
ClinVar RCV Id: RCV002423274 RCV002041099
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Met1Val