Canonical Allele Identifier: PA2827399631
Gene: A2M HGNC NCBI

Linked Data

ClinVar Variation Id: 2514869
ClinVar RCV Id: RCV004291448

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001334354.2:p.Pro429Ala
CA6438588
NM_001347425.2:c.1285C>G