Allele Registry

Canonical Allele Identifier: PA278259

Gene: BTD HGNC NCBI

ClinVar Allele:

36377

ClinVar RCV:

RCV000021962

ClinVar Variation:

25040

HGVS (amino-acid)	Matching Registered Transcripts
NP_000051.1:p.Ile255Thr	CA278258 NM_000060.4:c.764T>C