Allele Registry

Canonical Allele Identifier: PA2826204703

Gene: SPTAN1 HGNC NCBI

ClinVar RCV:

RCV000636363

ClinVar Variation:

530483

HGVS (amino-acid)	Matching Registered Transcripts
NP_001182461.1:p.Lys2313Glu	CA375099898 NM_001195532.2:c.6937A>G