Canonical Allele Identifier: PA124761
Gene: HBB HGNC NCBI

Linked Data

ClinVar Variation Id: 15116
ClinVar RCV Id: RCV000016271 RCV000641413
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000509.1:p.Pro101Leu
CA124760
NM_000518.5:c.302C>T