Canonical Allele Identifier: PA125621
Gene: HBA2 HGNC NCBI

Linked Data

ClinVar Variation Id: 15666
ClinVar RCV Id: RCV000016952
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000508.1:p.Ala27Val
CA125620
NM_000517.6:c.80C>T