Canonical Allele Identifier: PA124782
Gene: HBB HGNC NCBI

Linked Data

ClinVar Variation Id: 15130
ClinVar RCV Id: RCV000016293
ClinVar Variation Id: 15525
ClinVar RCV Id: RCV000016789 RCV000508224
ClinVar Variation Id: 439779
ClinVar RCV Id: RCV000506907
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000509.1:p.Arg105Ser
CA125395
NM_000518.5:c.315G>C
CA217113401
NM_000518.5:c.315G>T