ClinGen Allele Registry
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Canonical Allele Identifier:
PA318770
Gene: SPTAN1
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000189545
RCV000416988
RCV001195886
ClinVar Variation:
207370
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001123910.1:p.Arg2308_Met2309dup
CA318769
NM_001130438.3:c.6923_6928dup