Canonical Allele Identifier: PA199241
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_055637.2:p.Gln978Pro
CA199240
NM_014822.4:c.2933A>C