Canonical Allele Identifier: PA202847
Gene: EVC HGNC NCBI

Linked Data

ClinVar Variation Id: 197384

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_714928.1:p.Pro157Ala
CA202846
NM_153717.3:c.469C>G