Canonical Allele Identifier: PA2826910052
Gene: EVC HGNC NCBI

Linked Data

ClinVar Variation Id: 349210

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001293019.1:p.Gly957Arg
CA2836717
NM_001306090.2:c.2869G>A
CA2836718
NM_001306090.2:c.2869G>C