Allele Registry

Canonical Allele Identifier: PA127893

Gene: ALB HGNC NCBI

ClinVar RCV:

RCV000019835

RCV001154833

ClinVar Variation:

18192

HGVS (amino-acid)	Matching Registered Transcripts
NP_000468.1:p.Lys337Asn	CA127892 NM_000477.7:c.1011G>T CA99705776 NM_000477.7:c.1011G>C