Canonical Allele Identifier: PA2825820708
Gene: ERG HGNC NCBI
ClinVar RCV:
RCV004380570
ClinVar Variation:
3090151
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001129626.1:p.Pro261Ser
CA409943825
NM_001136154.1:c.781C>T