Canonical Allele Identifier: PA2580127162
Gene: HOXA13 HGNC NCBI

Linked Data

ClinVar Variation Id: 2432524
ClinVar RCV Id: RCV003135613
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000513.2:p.Ala45Thr
CA367076125
NM_000522.5:c.133G>A