Canonical Allele Identifier: PA2829858290
Gene: SEPSECS HGNC NCBI

Linked Data

ClinVar Variation Id: 3160013
ClinVar RCV Id: RCV004452915
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_058651.3:p.Leu113Phe
CA2877476
NM_016955.3:c.337C>T