Canonical Allele Identifier: PA645463101
Gene: BTD HGNC NCBI

Linked Data

ClinVar Variation Id: 429412
ClinVar RCV Id: RCV000492955 RCV000689556
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000051.1:p.Gly293Arg
CA2277389
NM_000060.4:c.877G>C