Allele Registry

Canonical Allele Identifier: PA658679406

Gene: SPTAN1 HGNC NCBI

ClinVar RCV:

RCV000539013

ClinVar Variation:

461231

HGVS (amino-acid)	Matching Registered Transcripts
NP_001123910.1:p.Lys1968Asn	CA5265591 NM_001130438.3:c.5904A>T CA375082360 NM_001130438.3:c.5904A>C