Canonical Allele Identifier: PA2828575836
Gene: SPTAN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 530408

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001362242.1:p.Ala858Ser
CA375058064
NM_001375313.1:c.2572G>T