Canonical Allele Identifier: PA2826589785
Gene: BTD HGNC NCBI

Linked Data

ClinVar Variation Id: 381650
ClinVar RCV Id: RCV000420327 RCV000675128 RCV001251699 RCV001731677 RCV004022351
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268652.2:p.Asp202Asn
CA2277359
NM_001281723.3:c.604G>A