Canonical Allele Identifier: PA2825028206
Gene: BTD HGNC NCBI

Linked Data

ClinVar Variation Id: 801135
ClinVar RCV Id: RCV000985646
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000051.1:p.Asp151Gly
CA2277312
NM_000060.4:c.452A>G