Allele Registry

Canonical Allele Identifier: PA278153

Gene: BTD HGNC NCBI

ClinVar Allele:

46846

ClinVar RCV:

RCV000021895

ClinVar Variation:

38487

HGVS (amino-acid)	Matching Registered Transcripts
NP_000051.1:p.Val62Met	CA278152 NM_000060.4:c.184G>A