Canonical Allele Identifier: PA645418157
Gene: SPTA1 HGNC NCBI

Linked Data

ClinVar Variation Id: 292938

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003117.2:p.Lys2331Glu
CA1181749
NM_003126.2:c.6991A>G