Canonical Allele Identifier: PA2826592265
Gene: BTD HGNC NCBI

Linked Data

ClinVar Variation Id: 25091
ClinVar RCV Id: RCV000434827
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268654.1:p.Trp467Arg
CA278344
NM_001281725.2:c.1399T>C
CA351608934
NM_001281725.2:c.1399T>A