Canonical Allele Identifier: PA658666020
Gene: EVC HGNC NCBI

Linked Data

ClinVar Variation Id: 446659

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_714928.1:p.Met500Ile
CA2836142
NM_153717.3:c.1500G>A
CA356157475
NM_153717.3:c.1500G>C
CA356157477
NM_153717.3:c.1500G>T