Canonical Allele Identifier: PA278345
Gene: BTD HGNC NCBI

Linked Data

ClinVar Variation Id: 25091
ClinVar RCV Id: RCV000434827
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000051.1:p.Trp487Arg
CA278344
NM_000060.4:c.1459T>C
CA351608934
NM_000060.4:c.1459T>A