Allele Registry

Canonical Allele Identifier: PA278396

Gene: BTD HGNC NCBI

ClinVar RCV:

RCV000032022

RCV000520641

ClinVar Variation:

38579

HGVS (amino-acid)	Matching Registered Transcripts
NP_000051.1:p.Asn214Ser	CA278395 NM_000060.4:c.641A>G