Canonical Allele Identifier: PA2828449105
Gene: BTD HGNC NCBI

Linked Data

ClinVar Variation Id: 2499909
ClinVar RCV Id: RCV003224001
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357681.1:p.Ser299Phe
CA351607571
NM_001370752.1:c.896C>T