Canonical Allele Identifier: PA2827399519
Gene: A2M HGNC NCBI

Linked Data

ClinVar Variation Id: 2376401
ClinVar RCV Id: RCV004215624

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001334352.2:p.Lys1003Thr
CA6438237
NM_001347423.2:c.3008A>C