Canonical Allele Identifier: PA1139708154
Gene: HOXB13 HGNC NCBI

Linked Data

ClinVar Variation Id: 943647
ClinVar RCV Id: RCV001213881
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006352.2:p.Ala282Thr
CA8633898
NM_006361.6:c.844G>A