Canonical Allele Identifier: PA123393
Gene: PRF1 HGNC NCBI
ClinVar Allele:
28758
ClinVar RCV:
RCV000014722
ClinVar Variation:
13719
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001076585.1:p.Ser388Ile
CA123391
NM_001083116.3:c.1163G>T