Canonical Allele Identifier: PA2829772059
Gene: SEC24D HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055637.2:p.Ser862Leu
CA358005041
NM_014822.4:c.2585C>T