Canonical Allele Identifier: PA124619
Gene: HBG1 HGNC NCBI

Linked Data

ClinVar Variation Id: 15027
ClinVar RCV Id: RCV000016168
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000550.2:p.Asp74His
CA124618
NM_000559.3:c.220G>C