Canonical Allele Identifier: PA2741984512
Gene: PRAMEF2 HGNC NCBI

Linked Data

ClinVar Variation Id: 3025679
ClinVar RCV Id: RCV003885067
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_075390.1:p.Pro117Ser
CA607989
NM_023014.1:c.349C>T