Canonical Allele Identifier: PA2827399660
Gene: A2M HGNC NCBI

Linked Data

ClinVar Variation Id: 2376401
ClinVar RCV Id: RCV004215624

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001334354.2:p.Lys853Thr
CA6438237
NM_001347425.2:c.2558A>C