Allele Registry

Canonical Allele Identifier: PA127926

Gene: ALB HGNC NCBI

ClinVar RCV:

RCV000019868

ClinVar Variation:

18209

HGVS (amino-acid)	Matching Registered Transcripts
NP_000468.1:p.Lys598Asn	CA99712628 NM_000477.7:c.1794A>T CA99712629 NM_000477.7:c.1794A>C