Canonical Allele Identifier: PA658712814
Gene: HOXD13 HGNC NCBI

Linked Data

ClinVar Variation Id: 493303
ClinVar RCV Id: RCV000584868 RCV002483560 RCV004553302
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000514.2:p.Pro99Arg
CA1976569
NM_000523.4:c.296C>G