Canonical Allele Identifier: PA2827399680
Gene: A2M HGNC NCBI

Linked Data

ClinVar Variation Id: 2205638
ClinVar RCV Id: RCV004069537

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001334354.2:p.Thr1305Met
CA6437891
NM_001347425.2:c.3914C>T