Canonical Allele Identifier: PA278365
Gene: BTD HGNC NCBI

Linked Data

ClinVar Variation Id: 38483
ClinVar RCV Id: RCV000022030 RCV001251701 RCV002513289
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000051.1:p.His43Arg
CA278364
NM_000060.4:c.128A>G