Canonical Allele Identifier: PA2573169860
Gene: ALB HGNC NCBI

Linked Data

ClinVar Variation Id: 1416088
ClinVar RCV Id: RCV001921157
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000468.1:p.His91Arg
CA2959336
NM_000477.7:c.272A>G