Canonical Allele Identifier: PA2825588408
Gene: RPTN HGNC NCBI

Linked Data

ClinVar Variation Id: 3156309
ClinVar RCV Id: RCV004452187
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001116437.1:p.Thr322Met
CA1099614
NM_001122965.1:c.965C>T