Allele Registry

Canonical Allele Identifier: PA2827195806

Gene: BTD HGNC NCBI

ClinVar RCV:

RCV000021961

ClinVar Variation:

25039

HGVS (amino-acid)	Matching Registered Transcripts
NP_001310511.1:p.Pro233Ser	CA278256 NM_001323582.1:c.697C>T