Canonical Allele Identifier: PA2741860554
Gene: A2M HGNC NCBI

Linked Data

ClinVar Variation Id: 3041387
ClinVar RCV Id: RCV003929799
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001334352.2:p.Leu18Arg
CA6439083
NM_001347423.2:c.53T>G