Allele Registry

Canonical Allele Identifier: PA2829297570

Gene: SLC4A11 HGNC NCBI

ClinVar RCV:

RCV002293386

ClinVar Variation:

1711855

HGVS (amino-acid)	Matching Registered Transcripts
NP_001387206.1:p.Ser454Trp	CA408088510 NM_001400277.1:c.1361C>G