ClinGen Allele Registry
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Canonical Allele Identifier:
PA2826204322
Gene: SPTAN1
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000443505
RCV001041521
RCV001808815
RCV004022391
ClinVar Variation:
385053
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001182461.1:p.Pro1798Leu
CA5265459
NM_001195532.2:c.5393C>T