Canonical Allele Identifier: PA2828113311
Gene: SPTAN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1333719
ClinVar RCV Id: RCV001808934
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350694.1:p.Gly1778Cys
CA375075946
NM_001363765.2:c.5332G>T