Canonical Allele Identifier: PA916077976
Gene: AUP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 337118
ClinVar RCV Id: RCV000354717 RCV004021819
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_853553.1:p.Pro9Ser
CA1728227
NM_181575.5:c.25C>T