Canonical Allele Identifier: PA109210
Gene: HOXB13 HGNC NCBI

Linked Data

ClinVar Variation Id: 128031
ClinVar RCV Id: RCV000210093 RCV000229815 RCV000561749 RCV000714291 RCV001582580 RCV004549575 RCV003492500 RCV001391199 RCV003335105
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006352.2:p.Gly84Glu
CA288225
NM_006361.6:c.251G>A