Canonical Allele Identifier: PA2825208038
Gene: HOXD13 HGNC NCBI

Linked Data

ClinVar Variation Id: 3106741
ClinVar RCV Id: RCV004402113

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000514.2:p.Gln248His
CA349353403
NM_000523.4:c.744G>C
CA349353404
NM_000523.4:c.744G>T