Canonical Allele Identifier: PA2825003030
Gene: A2M HGNC NCBI

Linked Data

ClinVar Variation Id: 2376401
ClinVar RCV Id: RCV004215624
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000005.3:p.Lys1003Thr
CA6438237
NM_000014.6:c.3008A>C