Canonical Allele Identifier: PA278436
Gene: BTD HGNC NCBI

Linked Data

ClinVar Variation Id: 156001
ClinVar RCV Id: RCV000144057 RCV000985647
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000051.1:p.Thr152Arg
CA278435
NM_000060.4:c.455C>G