Allele Registry

Canonical Allele Identifier: PA278271

Gene: BTD HGNC NCBI

ClinVar RCV:

RCV000021969

RCV000224487

RCV002265566

RCV003964809

ClinVar Variation:

25047

HGVS (amino-acid)	Matching Registered Transcripts
NP_000051.1:p.Ile294Val	CA278270 NM_000060.4:c.880A>G