Allele Registry

Canonical Allele Identifier: PA127958

Gene: ALB HGNC NCBI

ClinVar RCV:

RCV000019889

ClinVar Variation:

18228

HGVS (amino-acid)	Matching Registered Transcripts
NP_000468.1:p.Lys300Asn	CA127957 NM_000477.7:c.900G>C CA99705564 NM_000477.7:c.900G>T