Canonical Allele Identifier: PA124988
Gene: HBB HGNC NCBI

Linked Data

ClinVar Variation Id: 15241
ClinVar RCV Id: RCV000016443 RCV000016446 RCV001811157 RCV001826464
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000509.1:p.Val99Met
CA124987
NM_000518.5:c.295G>A