Canonical Allele Identifier: PA2580198994
Gene: SEC24D HGNC NCBI
ClinVar RCV:
RCV002685769
ClinVar Variation:
1948481
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001304995.1:p.Tyr821Asn
CA358005725
NM_001318066.2:c.2461T>A