Allele Registry

Canonical Allele Identifier: PA108697

Gene: SPTA1 HGNC NCBI

ClinVar RCV:

RCV000013707

RCV001508009

ClinVar Variation:

12853

HGVS (amino-acid)	Matching Registered Transcripts
NP_003117.2:p.Arg28Leu	CA122756 NM_003126.2:c.83G>T