Canonical Allele Identifier: PA658674558
Gene: HOXB13 HGNC NCBI

Linked Data

ClinVar Variation Id: 483529
ClinVar RCV Id: RCV000574760 RCV001051704
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006352.2:p.Arg258His
CA291348898
NM_006361.6:c.773G>A