Canonical Allele Identifier: PA278292
Gene: BTD HGNC NCBI

Linked Data

ClinVar Variation Id: 25059
ClinVar RCV Id: RCV000021982
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000051.1:p.Pro369Leu
CA278291
NM_000060.4:c.1106C>T