ClinGen Allele Registry
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Canonical Allele Identifier:
PA2828110197
Gene: SPTAN1
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000189428
RCV000528432
RCV001808475
ClinVar Variation:
207259
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001350688.1:p.Ala288Pro
CA318558
NM_001363759.2:c.862G>C