Canonical Allele Identifier: PA180004
Gene: EVC HGNC NCBI

Linked Data

ClinVar Variation Id: 167043

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_714928.1:p.Phe440Leu
CA180003
NM_153717.3:c.1320T>A
CA356155671
NM_153717.3:c.1318T>C
CA356155679
NM_153717.3:c.1320T>G