ClinGen Allele Registry
Allele Registry
Register
Login
Forgot Login?
Canonical Allele Identifier:
PA129892
Gene: B2M
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar Allele:
40563
ClinVar RCV:
RCV000024598
RCV000989305
ClinVar Variation:
31907
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_004039.1:p.Asp96Asn
CA129891
NM_004048.4:c.286G>A