Canonical Allele Identifier: PA2573170740
Gene: HOXA13 HGNC NCBI

Linked Data

ClinVar Variation Id: 1685262
ClinVar RCV Id: RCV002248989 RCV003933709
ClinVar Variation Id: 2821787
ClinVar RCV Id: RCV003711799
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000513.2:p.Ala133del
CA3004263435
NM_000522.5:c.397_399del