Canonical Allele Identifier: PA2826592173
Gene: BTD HGNC NCBI

Linked Data

ClinVar Variation Id: 809438
ClinVar RCV Id: RCV000998009 RCV003444022
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268654.1:p.Leu420Pro
CA351608540
NM_001281725.2:c.1259T>C