Canonical Allele Identifier: PA127963
Gene: ALB HGNC NCBI
ClinVar RCV:
RCV000019892
ClinVar Variation:
18231
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000468.1:p.Asp87Asn
CA127962
NM_000477.7:c.259G>A