Allele Registry

Canonical Allele Identifier: PA2827195930

Gene: BTD HGNC NCBI

ClinVar Allele:

36398

ClinVar RCV:

RCV000021987

RCV000405919

RCV002281714

ClinVar Variation:

25062

HGVS (amino-acid)	Matching Registered Transcripts
NP_001310511.1:p.Asn382Ser	CA278298 NM_001323582.1:c.1145A>G