Allele Registry

Canonical Allele Identifier: PA658673795

Gene: BTD HGNC NCBI

ClinVar RCV:

RCV000537387

RCV001591206

RCV001778993

RCV002527692

ClinVar Variation:

458809

HGVS (amino-acid)	Matching Registered Transcripts
NP_000051.1:p.Arg209Cys	CA2277351 NM_000060.4:c.625C>T