Canonical Allele Identifier: PA2826313975
Gene: PARN HGNC NCBI

Linked Data

ClinVar Variation Id: 423824
ClinVar RCV Id: RCV000484657 RCV001308486 RCV002509408
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001229921.1:p.Arg398Cys
CA7912056
NM_001242992.2:c.1192C>T