Canonical Allele Identifier: PA2829657670
Gene: SEC23B HGNC NCBI

Linked Data

ClinVar Variation Id: 2431450
ClinVar RCV Id: RCV003140504

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006354.2:p.Phe534Leu
CA312406964
NM_006363.6:c.1602C>G
CA408364125
NM_006363.6:c.1600T>C
CA408364130
NM_006363.6:c.1602C>A