Canonical Allele Identifier: PA2826204301
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_001182461.1:p.Gly1773Cys
CA375075946
NM_001195532.2:c.5317G>T