Canonical Allele Identifier: PA2825823035
Gene: EGR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1462789
ClinVar RCV Id: RCV001994908

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001129651.1:p.Ser378Arg
CA5517162
NM_001136179.1:c.1134C>A
CA377027180
NM_001136179.1:c.1134C>G
CA377027186
NM_001136179.1:c.1132A>C