Allele Registry

Canonical Allele Identifier: PA2825003029

Gene: A2M HGNC NCBI

ClinVar RCV:

RCV000019801

RCV001618215

ClinVar Variation:

18171

HGVS (amino-acid)	Matching Registered Transcripts
NP_000005.3:p.Ile1000Val	CA127858 NM_000014.6:c.2998A>G