Canonical Allele Identifier: PA2580127229
Gene: HOXD13 HGNC NCBI

Linked Data

ClinVar Variation Id: 1695392
ClinVar RCV Id: RCV002264894
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000514.2:p.Asp208Val
CA349353130
NM_000523.4:c.623A>T