Canonical Allele Identifier: PA2828446082
Gene: BTD HGNC NCBI

Linked Data

ClinVar Variation Id: 2043400
ClinVar RCV Id: RCV002912966
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357587.1:p.Gly323Val
CA2277409
NM_001370658.1:c.968G>T