Canonical Allele Identifier: PA170821
Gene: ALB HGNC NCBI

Linked Data

ClinVar Variation Id: 156315
ClinVar RCV Id: RCV000144399
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000468.1:p.Asp574Ala
CA170820
NM_000477.7:c.1721A>C