Canonical Allele Identifier: PA2826163951
Gene: RERG HGNC NCBI

Linked Data

ClinVar Variation Id: 522885
ClinVar RCV Id: RCV000626076
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001177655.1:p.Tyr65His
CA384055988
NM_001190726.2:c.193T>C