Canonical Allele Identifier: PA2827399567
Gene: A2M HGNC NCBI

Linked Data

ClinVar Variation Id: 18174
ClinVar RCV Id: RCV000019805
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001334353.2:p.Arg604His
CA127863
NM_001347424.2:c.1811G>A