Canonical Allele Identifier: PA127889
Gene: ALB HGNC NCBI

Linked Data

ClinVar Variation Id: 18190
ClinVar RCV Id: RCV000019831
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000468.1:p.Glu143Lys
CA127888
NM_000477.7:c.427G>A