Allele Registry

Canonical Allele Identifier: PA278167

Gene: BTD HGNC NCBI

ClinVar Allele:

46851

ClinVar RCV:

RCV000021905

RCV003125847

RCV003993755

ClinVar Variation:

38567

HGVS (amino-acid)	Matching Registered Transcripts
NP_000051.1:p.Arg79His	CA278166 NM_000060.4:c.236G>A