Canonical Allele Identifier: PA2826590459
Gene: BTD HGNC NCBI

Linked Data

ClinVar Variation Id: 24989
ClinVar RCV Id: RCV000021907 RCV001171830 RCV001800312
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268653.2:p.Ala62Val
CA278170
NM_001281724.3:c.185C>T