Canonical Allele Identifier: PA099807
Gene: HOXD13 HGNC NCBI

Linked Data

ClinVar Variation Id: 14874
ClinVar RCV Id: RCV000016002
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000514.2:p.Gln325Arg
CA124418
NM_000523.4:c.974A>G