Canonical Allele Identifier: PA1139676730
Gene: ALB HGNC NCBI

Linked Data

ClinVar Variation Id: 904664
ClinVar RCV Id: RCV001152706

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000468.1:p.Ala83Val
CA2959316
NM_000477.7:c.248C>T