Canonical Allele Identifier: PA127903
Gene: ALB HGNC NCBI

Linked Data

ClinVar Variation Id: 18197
ClinVar RCV Id: RCV000019842
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000468.1:p.Asp389His
CA127902
NM_000477.7:c.1165G>C