ClinGen Allele Registry
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Canonical Allele Identifier:
PA1139741949
Gene: SPTAN1
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000147650
RCV000189543
RCV001236667
RCV004551284
ClinVar Variation:
160024
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001350688.1:p.Glu2207del
CA173593
NM_001363759.2:c.6619_6621del