Canonical Allele Identifier: PA125075
Gene: HBB HGNC NCBI

Linked Data

ClinVar Variation Id: 15294
ClinVar RCV Id: RCV000016527 RCV000641554
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000509.1:p.Ala143Asp
CA125074
NM_000518.5:c.428C>A