Canonical Allele Identifier: PA2580198992
Gene: SEC24D HGNC NCBI

Linked Data

ClinVar Variation Id: 2100891
ClinVar RCV Id: RCV003025994
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001304995.1:p.Pro802Ser
CA358006130
NM_001318066.2:c.2404C>T