ClinGen Allele Registry
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Canonical Allele Identifier:
PA915981319
Gene: SPTAN1
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000636326
RCV000727121
RCV001808507
ClinVar Variation:
207315
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_003118.2:p.Arg320His
CA318662
NM_003127.4:c.959G>A