Canonical Allele Identifier: PA2825237071
Gene: RUNX1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1439732
ClinVar RCV Id: RCV001936692

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001001890.1:p.Val91Leu
CA410202790
NM_001001890.3:c.271G>T
CA410202791
NM_001001890.3:c.271G>C