Canonical Allele Identifier: PA278396
Gene: BTD HGNC NCBI

Linked Data

ClinVar Variation Id: 38579
ClinVar RCV Id: RCV000032022 RCV000520641
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000051.1:p.Asn214Ser
CA278395
NM_000060.4:c.641A>G