Canonical Allele Identifier: PA2826910392
Gene: EVC HGNC NCBI

Linked Data

ClinVar Variation Id: 5343

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001293021.1:p.Ser307Pro
CA117420
NM_001306092.2:c.919T>C