Canonical Allele Identifier: PA645468370
Gene: B2M HGNC NCBI

Linked Data

ClinVar Variation Id: 376368
ClinVar RCV Id: RCV000422802 RCV000426129 RCV000423896 RCV000430927 RCV000432370 RCV000433517 RCV000433775 RCV000441172 RCV000442543 RCV000442680
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004039.1:p.Met1Ile