Canonical Allele Identifier: PA2580370851
Gene: HOXC11 HGNC NCBI

Linked Data

ClinVar Variation Id: 2463478
ClinVar RCV Id: RCV004262402
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055027.1:p.Glu168Lys
CA6604255
NM_014212.4:c.502G>A