Canonical Allele Identifier: PA2826590870
Gene: BTD HGNC NCBI

Linked Data

ClinVar Variation Id: 25044
ClinVar RCV Id: RCV000021966
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268653.2:p.Leu258Val
CA278264
NM_001281724.3:c.772C>G