Allele Registry

Canonical Allele Identifier: PA278357

Gene: BTD HGNC NCBI

ClinVar RCV:

RCV000022024

ClinVar Variation:

25099

HGVS (amino-acid)	Matching Registered Transcripts
NP_000051.1:p.Arg538His	CA278356 NM_000060.4:c.1613G>A