Canonical Allele Identifier: PA658674578
Gene: HOXB13 HGNC NCBI

Linked Data

ClinVar Variation Id: 483500
ClinVar RCV Id: RCV000572382 RCV001368332
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006352.2:p.Arg268Gln
CA8633906
NM_006361.6:c.803G>A