Canonical Allele Identifier: PA2580370855
Gene: HOXC11 HGNC NCBI

Linked Data

ClinVar Variation Id: 2228996
ClinVar RCV Id: RCV004096948
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055027.1:p.Arg192Gly
CA6604273
NM_014212.4:c.574C>G