Canonical Allele Identifier: PA125016
Gene: HBB HGNC NCBI

Linked Data

ClinVar Variation Id: 15258
ClinVar RCV Id: RCV000016479 RCV000016480 RCV000016481 RCV000020338 RCV000508637 RCV001000121
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000509.1:p.Asn20Ser
CA125015
NM_000518.5:c.59A>G