Allele Registry

Canonical Allele Identifier: PA916048679

Gene: BTD HGNC NCBI

ClinVar RCV:

RCV000021969

RCV000224487

RCV002265566

RCV003964809

ClinVar Variation:

25047

HGVS (amino-acid)	Matching Registered Transcripts
NP_001357681.1:p.Ile274Val	CA278270 NM_001370752.1:c.820A>G