Canonical Allele Identifier: PA2826327654
Gene: ERG HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230357.1:p.Pro261Ser
CA409943825
NM_001243428.1:c.781C>T