Canonical Allele Identifier: PA2826203690
Gene: SPTAN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 530408

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001182461.1:p.Ala858Ser
CA375058064
NM_001195532.2:c.2572G>T