Canonical Allele Identifier: PA915978018
Gene: EGR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 16750
ClinVar RCV Id: RCV001049422 RCV003482227 RCV000018234
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001129650.1:p.Arg409Trp
CA341431
NM_001136178.1:c.1225C>T