Canonical Allele Identifier: PA2826909640
Gene: EVC HGNC NCBI

Linked Data

ClinVar Variation Id: 446659

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001293019.1:p.Met500Ile
CA2836142
NM_001306090.2:c.1500G>A
CA356157475
NM_001306090.2:c.1500G>C
CA356157477
NM_001306090.2:c.1500G>T