Canonical Allele Identifier: PA2829772155
Gene: SEC24D HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055637.2:p.Val1005Gly
CA358003403
NM_014822.4:c.3014T>G