Allele Registry

Canonical Allele Identifier: PA278226

Gene: BTD HGNC NCBI

ClinVar RCV:

RCV000021942

RCV000727575

RCV002298448

ClinVar Variation:

25021

HGVS (amino-acid)	Matching Registered Transcripts
NP_000051.1:p.Asn195Asp	CA278225 NM_000060.4:c.583A>G