Canonical Allele Identifier: PA645496203
Gene: EVC HGNC NCBI

Linked Data

ClinVar Variation Id: 287369

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_714928.1:p.Ala450Val
CA2836076
NM_153717.3:c.1349C>T