Canonical Allele Identifier: PA2741984514
Gene: PRAMEF2 HGNC NCBI

Linked Data

ClinVar Variation Id: 3025685
ClinVar RCV Id: RCV003885073
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_075390.1:p.Ala119Ser
CA607993
NM_023014.1:c.355G>T