Canonical Allele Identifier: PA2827195896
Gene: BTD HGNC NCBI

Linked Data

ClinVar Variation Id: 975025
ClinVar RCV Id: RCV001251432
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001310511.1:p.Phe341Val
CA351608028
NM_001323582.1:c.1021T>G