Allele Registry

Canonical Allele Identifier: PA127935

Gene: ALB HGNC NCBI

ClinVar RCV:

RCV000019875

ClinVar Variation:

18215

HGVS (amino-acid)	Matching Registered Transcripts
NP_000468.1:p.Cys201Phe	CA127934 NM_000477.7:c.602G>T