Canonical Allele Identifier: PA2827399557
Gene: A2M HGNC NCBI

Linked Data

ClinVar Variation Id: 2514869
ClinVar RCV Id: RCV004291448

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001334353.2:p.Pro479Ala
CA6438588
NM_001347424.2:c.1435C>G