ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA318685
Gene: SPTAN1
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000189499
RCV001302124
RCV001808512
ClinVar Variation:
207326
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001123910.1:p.Arg801Gln
CA318684
NM_001130438.3:c.2402G>A