Allele Registry

Canonical Allele Identifier: PA278436

Gene: BTD HGNC NCBI

ClinVar Allele:

165805

ClinVar RCV:

RCV000144057

RCV000985647

ClinVar Variation:

156001

HGVS (amino-acid)	Matching Registered Transcripts
NP_000051.1:p.Thr152Arg	CA278435 NM_000060.4:c.455C>G