Canonical Allele Identifier: PA2828110772
Gene: SPTAN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 745446
ClinVar RCV Id: RCV000921987
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350688.1:p.Tyr918Asn
CA375058545
NM_001363759.2:c.2752T>A