Allele Registry

Canonical Allele Identifier: PA2827399659

Gene: A2M HGNC NCBI

ClinVar RCV:

RCV000019801

RCV001618215

ClinVar Variation:

18171

HGVS (amino-acid)	Matching Registered Transcripts
NP_001334354.2:p.Ile850Val	CA127858 NM_001347425.2:c.2548A>G