Canonical Allele Identifier: PA2828574550
Gene: SPTAN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 530408

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001362241.2:p.Ala870Ser
CA375058064
NM_001375312.2:c.2608G>T