Canonical Allele Identifier: PA891863897
Gene: HOXD13 HGNC NCBI

Linked Data

ClinVar Variation Id: 591240
ClinVar RCV Id: RCV000722418

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000514.2:p.Ser225Cys
CA60846579
NM_000523.4:c.674C>G