Allele Registry

Canonical Allele Identifier: PA127905

Gene: ALB HGNC NCBI

ClinVar RCV:

RCV000019844

ClinVar Variation:

18198

HGVS (amino-acid)	Matching Registered Transcripts
NP_000468.1:p.Lys396Glu	CA127904 NM_000477.7:c.1186A>G