Canonical Allele Identifier: PA2741816335
Gene: HOXD13 HGNC NCBI

Linked Data

ClinVar Variation Id: 2818313
ClinVar RCV Id: RCV003713654
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000514.2:p.Gly261Arg
CA349353486
NM_000523.4:c.781G>A
CA349353487
NM_000523.4:c.781G>C