Allele Registry

Canonical Allele Identifier: PA127921

Gene: ALB HGNC NCBI

ClinVar RCV:

RCV000019859

ClinVar Variation:

18206

HGVS (amino-acid)	Matching Registered Transcripts
NP_000468.1:p.Glu589Lys	CA127920 NM_000477.7:c.1765G>A