ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA112868
Gene: SGCB
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000009256
ClinVar Variation:
8718
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_000223.1:p.Met100Lys
CA119858
NM_000232.5:c.299T>A