Allele Registry

Canonical Allele Identifier: PA645468368

Gene: B2M HGNC NCBI

Linked Data - NCBI & NCI

ClinVar RCV:

RCV000421861

RCV000422880

RCV000425118

RCV000430300

RCV000431428

RCV000432545

RCV000432685

RCV000439880

RCV000440097

RCV000441906

RCV005231520

ClinVar Variation:

376370

3764927

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_004039.1:p.Met1Leu