Canonical Allele Identifier: PA2825780932
Gene: PARN HGNC NCBI

Linked Data

ClinVar Variation Id: 542669
ClinVar RCV Id: RCV000653141 RCV000850488 RCV001816642 RCV002223900 RCV003447549 RCV003994067
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001127949.1:p.Tyr30Cys
CA7912470
NM_001134477.3:c.89A>G