Allele Registry

Canonical Allele Identifier: PA2580375746

Gene: SEC22A HGNC NCBI

ClinVar Allele:

2341901

ClinVar RCV:

RCV004184849

ClinVar Variation:

2348200

HGVS (amino-acid)	Matching Registered Transcripts
NP_036562.2:p.Ile178Met	CA2576539 NM_012430.5:c.534T>G