Canonical Allele Identifier: PA278162
Gene: BTD HGNC NCBI

Linked Data

ClinVar Variation Id: 38482
ClinVar RCV Id: RCV000021900 RCV000427971
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000051.1:p.Leu71Pro
CA278161
NM_000060.4:c.212T>C