ClinGen Allele Registry
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Canonical Allele Identifier:
PA915981618
Gene: SPTAN1
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar RCV:
RCV001721229
RCV001852510
ClinVar Variation:
207329
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_003118.2:p.Ala1027Thr
CA318690
NM_003127.4:c.3079G>A