Allele Registry

Canonical Allele Identifier: PA916062087

Gene: BGLAP HGNC NCBI

ClinVar RCV:

RCV000961307

ClinVar Variation:

780264

HGVS (amino-acid)	Matching Registered Transcripts
NP_954642.1:p.Arg94Gln	CA1156173 NM_199173.6:c.281G>A