Canonical Allele Identifier: PA658816965
Gene: PARN HGNC NCBI

Linked Data

ClinVar Variation Id: 542669
ClinVar RCV Id: RCV000653141 RCV000850488 RCV001816642 RCV002223900 RCV003447549 RCV003994067
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002573.1:p.Tyr91Cys
CA7912470
NM_002582.4:c.272A>G