Canonical Allele Identifier: PA2829772155
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_055637.2:p.Val1005Gly
CA358003403
NM_014822.4:c.3014T>G