Canonical Allele Identifier: PA278387
Gene: BTD HGNC NCBI

Linked Data

ClinVar Variation Id: 38574
ClinVar RCV Id: RCV000032017 RCV000506513
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000051.1:p.Glu64Asp
CA278386
NM_000060.4:c.192G>C
CA351603230
NM_000060.4:c.192G>T