Canonical Allele Identifier: PA2741816324
Gene: HOXD13 HGNC NCBI

Linked Data

ClinVar Variation Id: 2795109
ClinVar RCV Id: RCV003675237
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000514.2:p.Val203Met
CA349353098
NM_000523.4:c.607G>A