Canonical Allele Identifier: PA2580370852
Gene: HOXC11 HGNC NCBI

Linked Data

ClinVar Variation Id: 2383768
ClinVar RCV Id: RCV004219539
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055027.1:p.Gly175Ser
CA6604260
NM_014212.4:c.523G>A