ClinGen Allele Registry
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Canonical Allele Identifier:
PA2828112619
Gene: SPTAN1
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000189437
RCV000474925
RCV001705044
RCV001808482
RCV002426915
RCV004553030
ClinVar Variation:
207267
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001350694.1:p.Gln745Lys
CA318575
NM_001363765.2:c.2233C>A