Allele Registry

Canonical Allele Identifier: PA2826590994

Gene: BTD HGNC NCBI

ClinVar RCV:

RCV000022033

RCV000278976

ClinVar Variation:

25107

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268653.2:p.Asn329Thr	CA278370 NM_001281724.3:c.986A>C