ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA2829645372
Gene: SEPTIN9
HGNC
NCBI
Linked Data
ClinVar Variation Id:
2445583
ClinVar RCV Id:
RCV003154992
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_006631.2:p.Ser56Trp
CA401205740
NM_006640.5:c.167C>G