Canonical Allele Identifier: PA126002
Gene: HBA1 HGNC NCBI

Linked Data

ClinVar Variation Id: 15877
ClinVar RCV Id: RCV000017223
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000549.1:p.Val56Leu
CA126001
NM_000558.5:c.166G>C