Canonical Allele Identifier: PA2825781121
Gene: PARN HGNC NCBI

Linked Data

ClinVar Variation Id: 180661
ClinVar RCV Id: RCV000162313 RCV000170484
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001127949.1:p.Ala322Val
CA250319
NM_001134477.3:c.965C>T