Canonical Allele Identifier: PA2826909590
Gene: EVC HGNC NCBI

Linked Data

ClinVar Variation Id: 167043
ClinVar RCV Id: RCV000153203 RCV000397131 RCV000548805 RCV001795264
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001293019.1:p.Phe440Leu
CA180003
NM_001306090.2:c.1320T>A
CA356155671
NM_001306090.2:c.1318T>C
CA356155679
NM_001306090.2:c.1320T>G