Canonical Allele Identifier: PA2829417391
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_003118.2:p.Ala1860Asp
CA375077438
NM_003127.4:c.5579C>A