Allele Registry

Canonical Allele Identifier: PA645468367

Gene: B2M HGNC NCBI

Linked Data - NCBI & NCI

ClinVar RCV:

RCV000419044

RCV000419253

RCV000420355

RCV000426708

RCV000427508

RCV000429996

RCV000437364

RCV000438190

RCV000439772

RCV000444855

RCV005009638

ClinVar Variation:

376371

3577174

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_004039.1:p.Met1Thr