Canonical Allele Identifier: PA2825002969
Gene: A2M HGNC NCBI

Linked Data

ClinVar Variation Id: 3146264
ClinVar RCV Id: RCV004439650

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000005.3:p.Lys93Met
CA6439006
NM_000014.6:c.278A>T