Canonical Allele Identifier: PA2580207190
Gene: A2M HGNC NCBI

Linked Data

ClinVar Variation Id: 2264696
ClinVar RCV Id: RCV004116513

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001334353.2:p.Ile905Thr
CA6438236
NM_001347424.2:c.2714T>C