Allele Registry

Canonical Allele Identifier: PA093594

Gene: BTD HGNC NCBI

ClinVar Allele:

16936

ClinVar RCV:

RCV000001974

RCV000185809

ClinVar Variation:

1897

HGVS (amino-acid)	Matching Registered Transcripts
NP_000051.1:p.Thr532Met	CA278009 NM_000060.4:c.1595C>T