Canonical Allele Identifier: PA2826877259
Gene: TMED4 HGNC NCBI

Linked Data

ClinVar Variation Id: 3178357
ClinVar RCV Id: RCV004472746

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001289987.1:p.Ala6Val
CA157902940
NM_001303058.2:c.17C>T