Canonical Allele Identifier: PA2825236835
Gene: RUNX1 HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001001890.1:p.Ser46Arg
CA410203871
NM_001001890.3:c.138C>G
CA410203872
NM_001001890.3:c.138C>A
CA410203878
NM_001001890.3:c.136A>C