Allele Registry

Canonical Allele Identifier: PA2826590283

Gene: BTD HGNC NCBI

ClinVar RCV:

RCV000001980

RCV002272006

RCV003230341

ClinVar Variation:

1903

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268652.2:p.Asn469Thr	CA278014 NM_001281723.3:c.1406A>C