Canonical Allele Identifier: PA2826592270
Gene: BTD HGNC NCBI

Linked Data

ClinVar Variation Id: 1903
ClinVar RCV Id: RCV000001980 RCV003230341 RCV002272006
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268654.1:p.Asn469Thr
CA278014
NM_001281725.2:c.1406A>C