Allele Registry

Canonical Allele Identifier: PA916073964

Gene: SEC23B HGNC NCBI

ClinVar RCV:

RCV000275527

RCV000945938

RCV001509049

RCV004549773

ClinVar Variation:

337792

HGVS (amino-acid)	Matching Registered Transcripts
NP_116781.1:p.Phe400Leu	CA9778252 NM_032986.5:c.1198T>C CA408361773 NM_032986.5:c.1200C>A CA408361775 NM_032986.5:c.1200C>G