Canonical Allele Identifier: PA645496159
Gene: EVC HGNC NCBI

Linked Data

ClinVar Variation Id: 290794

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_714928.1:p.Pro30Leu
CA10606907
NM_153717.3:c.89C>T