Canonical Allele Identifier: PA342857
Gene: HBB HGNC NCBI

Linked Data

ClinVar Variation Id: 15326
ClinVar RCV Id: RCV000016566
ClinVar Variation Id: 36311
ClinVar RCV Id: RCV000589853 RCV001272124 RCV003387731
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000509.1:p.Asn103Lys
CA342856
NM_000518.5:c.309C>A
CA217113423
NM_000518.5:c.309C>G