Canonical Allele Identifier: PA916048694
Gene: BTD HGNC NCBI

Linked Data

ClinVar Variation Id: 25107
ClinVar RCV Id: RCV000022033 RCV000278976
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357681.1:p.Asn329Thr
CA278370
NM_001370752.1:c.986A>C