Canonical Allele Identifier: PA112369
Gene: HESX1 HGNC NCBI

Linked Data

ClinVar Variation Id: 7695
ClinVar RCV Id: RCV000008134
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003856.1:p.Ile26Thr
CA119002
NM_003865.3:c.77T>C