Canonical Allele Identifier: PA125218
Gene: HBB HGNC NCBI

Linked Data

ClinVar Variation Id: 15379
ClinVar RCV Id: RCV000016631
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000509.1:p.Pro125Ser
CA125217
NM_000518.5:c.373C>T