Canonical Allele Identifier: PA915977969
Gene: EGR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 16752
ClinVar RCV Id: RCV000018236 RCV000018237 RCV000032120 RCV000231023 RCV000498897 RCV000856959
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001129650.1:p.Arg359Trp
CA126845
NM_001136178.1:c.1075C>T