Allele Registry

Canonical Allele Identifier: PA113465

Gene: B2M HGNC NCBI

ClinVar RCV:

RCV000019314

ClinVar Variation:

17740

HGVS (amino-acid)	Matching Registered Transcripts
NP_004039.1:p.Ala11Pro	CA251327 NM_004048.4:c.31G>C