Canonical Allele Identifier: PA125930
Gene: HBA1 HGNC NCBI

Linked Data

ClinVar Variation Id: 15837
ClinVar RCV Id: RCV000017182
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000549.1:p.Lys57Asn
CA125929
NM_000558.5:c.171G>C
CA276416796
NM_000558.5:c.171G>T