Canonical Allele Identifier: PA1139689448
Gene: EGR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 839043
ClinVar RCV Id: RCV001040717
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001129650.1:p.Arg415Cys
CA377027273
NM_001136178.1:c.1243C>T