Allele Registry

Canonical Allele Identifier: PA915975048

Gene: HOXB13 HGNC NCBI

ClinVar RCV:

RCV000856508

RCV002298793

ClinVar Variation:

691205

HGVS (amino-acid)	Matching Registered Transcripts
NP_006352.2:p.Gln265His	CA400105644 NM_006361.6:c.795G>T CA400105649 NM_006361.6:c.795G>C