Canonical Allele Identifier: PA916022227
Gene: SEC24D HGNC NCBI

Linked Data

ClinVar Variation Id: 189341
ClinVar RCV Id: RCV000169757
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001304995.1:p.Gln979Pro
CA199240
NM_001318066.2:c.2936A>C