ClinGen Allele Registry
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Canonical Allele Identifier:
PA2828110349
Gene: SPTAN1
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000189432
RCV000463688
RCV001808478
ClinVar Variation:
207262
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001350688.1:p.Ala450Ser
CA318566
NM_001363759.2:c.1348G>T