ClinGen Allele Registry
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Canonical Allele Identifier:
PA2826204069
Gene: SPTAN1
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000189510
RCV000636442
RCV001808515
ClinVar Variation:
207336
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001182461.1:p.Arg1417His
CA318703
NM_001195532.2:c.4250G>A