ClinGen Allele Registry
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Canonical Allele Identifier:
PA2830110876
Gene: SEC23B
HGNC
NCBI
Linked Data
ClinVar Variation Id:
3064761
ClinVar RCV Id:
RCV003989246
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_116780.1:p.Gly301Asp
CA408360158
NM_032985.6:c.902G>A