Canonical Allele Identifier: PA2825820735
Gene: ERG HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001129627.1:p.Pro162Ser
CA409943825
NM_001136155.1:c.484C>T