Canonical Allele Identifier: PA2825003013
Gene: A2M HGNC NCBI

Linked Data

ClinVar Variation Id: 3143593
ClinVar RCV Id: RCV004436399
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000005.3:p.Ile762Met
CA6438423
NM_000014.6:c.2286C>G