Canonical Allele Identifier: PA2825588403
Gene: RPTN HGNC NCBI

Linked Data

ClinVar Variation Id: 3156303
ClinVar RCV Id: RCV004452181
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001116437.1:p.Arg151Ser
CA342043018
NM_001122965.1:c.453A>T
CA342043020
NM_001122965.1:c.453A>C