Canonical Allele Identifier: PA2827067739
Gene: EGR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1462789
ClinVar RCV Id: RCV001994908
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001307966.1:p.Ser378Arg
CA5517162
NM_001321037.2:c.1134C>A
CA377027180
NM_001321037.2:c.1134C>G
CA377027186
NM_001321037.2:c.1132A>C