ClinGen Allele Registry
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Canonical Allele Identifier:
PA2826079977
Gene: SEC23B
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000001283
RCV003480015
RCV003764507
ClinVar Variation:
1224
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001166217.1:p.Arg512Trp
CA114849
NM_001172746.3:c.1534C>T