Canonical Allele Identifier: PA2826591119
Gene: BTD HGNC NCBI

Linked Data

ClinVar Variation Id: 38577
ClinVar RCV Id: RCV000032020 RCV003480039
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268653.2:p.Gly393Ser
CA278392
NM_001281724.3:c.1177G>A