Canonical Allele Identifier: PA2829858419
Gene: SEPSECS HGNC NCBI

Linked Data

ClinVar Variation Id: 3160015
ClinVar RCV Id: RCV004452917
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_058651.3:p.Asp321Glu
CA356536888
NM_016955.3:c.963T>A
CA356536889
NM_016955.3:c.963T>G