ClinGen Allele Registry
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Canonical Allele Identifier:
PA915981237
Gene: SPTAN1
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000189484
RCV001439173
RCV001808503
ClinVar Variation:
207311
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_003118.2:p.Arg123His
CA318654
NM_003127.4:c.368G>A