Canonical Allele Identifier: PA658674479
Gene: HOXB13 HGNC NCBI

Linked Data

ClinVar Variation Id: 483499
ClinVar RCV Id: RCV000561971 RCV001858292
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006352.2:p.Ser93Ala
CA8634029
NM_006361.6:c.277T>G