Canonical Allele Identifier: PA2827399520
Gene: A2M HGNC NCBI

Linked Data

ClinVar Variation Id: 2264696
ClinVar RCV Id: RCV004116513
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001334352.2:p.Ile1005Thr
CA6438236
NM_001347423.2:c.3014T>C