Canonical Allele Identifier: PA645501898
Gene: EVC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 349078

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_667338.3:p.Ala616Thr
CA2834922
NM_147127.5:c.1846G>A