Canonical Allele Identifier: PA2826591005
Gene: BTD HGNC NCBI

Linked Data

ClinVar Variation Id: 1450085
ClinVar RCV Id: RCV001989965
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268653.2:p.His338Arg
CA351608005
NM_001281724.3:c.1013A>G