ClinGen Allele Registry
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Canonical Allele Identifier:
PA114845
Gene: SEC23B
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000001281
RCV000081407
RCV000688348
RCV004547453
ClinVar Variation:
1222
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_116780.1:p.Glu109Lys
CA114843
NM_032985.6:c.325G>A