Canonical Allele Identifier: PA2573249902
Gene: HOXB13 HGNC NCBI

Linked Data

ClinVar Variation Id: 1514664
ClinVar RCV Id: RCV002029463 RCV003161242
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006352.2:p.Ala282Val
CA400105171
NM_006361.6:c.845C>T