Canonical Allele Identifier: PA916044146
Gene: SPTAN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 661303
ClinVar RCV Id: RCV000818691
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350688.1:p.Ala1865Asp
CA375077438
NM_001363759.2:c.5594C>A