Allele Registry

Canonical Allele Identifier: PA108852

Gene: SPTA1 HGNC NCBI

ClinVar RCV:

RCV000013701

RCV002284170

ClinVar Variation:

12848

HGVS (amino-acid)	Matching Registered Transcripts
NP_003117.2:p.Ser261Pro	CA122751 NM_003126.2:c.781T>C