Canonical Allele Identifier: PA278310
Gene: BTD HGNC NCBI

Linked Data

ClinVar Variation Id: 25071
ClinVar RCV Id: RCV000021996
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000051.1:p.Cys418Ser
CA278309
NM_000060.4:c.1253G>C
CA351608402
NM_000060.4:c.1252T>A