ClinGen Allele Registry
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Canonical Allele Identifier:
PA2826204579
Gene: SPTAN1
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000440777
RCV002522382
ClinVar Variation:
387660
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001182461.1:p.Arg2135Cys
CA5265709
NM_001195532.2:c.6403C>T