Allele Registry

Canonical Allele Identifier: PA1139708126

Gene: HOXB13 HGNC NCBI

ClinVar RCV:

RCV001232474

RCV002418796

ClinVar Variation:

959177

HGVS (amino-acid)	Matching Registered Transcripts
NP_006352.2:p.Lys270Glu	CA400105517 NM_006361.6:c.808A>G