Allele Registry

Canonical Allele Identifier: PA2826591690

Gene: BTD HGNC NCBI

ClinVar RCV:

RCV000021942

RCV000727575

RCV002298448

ClinVar Variation:

25021

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268654.1:p.Asn175Asp	CA278225 NM_001281725.2:c.523A>G