Canonical Allele Identifier: PA916022326
Gene: BTBD16 HGNC NCBI

Linked Data

ClinVar Variation Id: 161806
ClinVar RCV Id: RCV000149342
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305118.1:p.Pro29Ser
CA174820
NM_001318189.1:c.85C>T