Allele Registry

Canonical Allele Identifier: PA127929

Gene: ALB HGNC NCBI

ClinVar RCV:

RCV000019871

ClinVar Variation:

18212

HGVS (amino-acid)	Matching Registered Transcripts
NP_000468.1:p.Lys560Glu	CA127928 NM_000477.7:c.1678A>G