Canonical Allele Identifier: PA2826590478
Gene: BTD HGNC NCBI

Linked Data

ClinVar Variation Id: 385308
ClinVar RCV Id: RCV000755884 RCV000876680 RCV002521735 RCV003912709
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268653.2:p.Gln68Glu
CA2277272
NM_001281724.3:c.202C>G