Canonical Allele Identifier: PA2826589764
Gene: BTD HGNC NCBI

Linked Data

ClinVar Variation Id: 38579
ClinVar RCV Id: RCV000032022 RCV000520641
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268652.2:p.Asn194Ser
CA278395
NM_001281723.3:c.581A>G