Canonical Allele Identifier: PA2829858276
Gene: SEPSECS HGNC NCBI

Linked Data

ClinVar Variation Id: 2466233
ClinVar RCV Id: RCV003190675
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_058651.3:p.Arg90Ser
CA2877488
NM_016955.3:c.270G>T
CA356542911
NM_016955.3:c.270G>C