Allele Registry

Canonical Allele Identifier: PA278336

Gene: BTD HGNC NCBI

ClinVar RCV:

RCV002651650

ClinVar Variation:

2203322

HGVS (amino-acid)	Matching Registered Transcripts
NP_000051.1:p.Val457Met	CA278335 NM_000060.4:c.1369G>A