Canonical Allele Identifier: PA2741860567
Gene: A2M HGNC NCBI

Linked Data

ClinVar Variation Id: 2514869
ClinVar RCV Id: RCV004291448
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001334352.2:p.Pro579Ala
CA6438588
NM_001347423.2:c.1735C>G