Canonical Allele Identifier: PA100614
Gene: SEPSECS HGNC NCBI

Linked Data

ClinVar Variation Id: 18400

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_058651.3:p.Tyr334Cys
CA114252
NM_016955.3:c.1001A>G