Canonical Allele Identifier: PA127358
Gene: ABO HGNC NCBI

Linked Data

ClinVar Variation Id: 17739
ClinVar RCV Id: RCV000019313
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_065202.2:p.Pro234Ala
CA127357
NM_020469.3:c.700C>G