Canonical Allele Identifier: PA645496633
Gene: EVC HGNC NCBI

Linked Data

ClinVar Variation Id: 349210

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_714928.1:p.Gly957Arg
CA2836717
NM_153717.3:c.2869G>A
CA2836718
NM_153717.3:c.2869G>C