Allele Registry

Canonical Allele Identifier: PA2573070780

Gene: A2M HGNC NCBI

ClinVar RCV:

RCV000019801

RCV001618215

ClinVar Variation:

18171

HGVS (amino-acid)	Matching Registered Transcripts
NP_001334353.2:p.Ile900Val	CA127858 NM_001347424.2:c.2698A>G