Allele Registry

Canonical Allele Identifier: PA278251

Gene: BTD HGNC NCBI

ClinVar RCV:

RCV000021958

ClinVar Variation:

25036

HGVS (amino-acid)	Matching Registered Transcripts
NP_000051.1:p.Ala237Thr	CA278250 NM_000060.4:c.709G>A