Canonical Allele Identifier: PA2573198651
Gene: SEC24D HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001304995.1:p.Ser863Leu
CA358005041
NM_001318066.2:c.2588C>T