Canonical Allele Identifier: PA2573198659
Gene: SEC24D HGNC NCBI

Linked Data

ClinVar Variation Id: 1345860
ClinVar RCV Id: RCV002037605
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001304995.1:p.Val1006Gly
CA358003403
NM_001318066.2:c.3017T>G