Canonical Allele Identifier: PA2826218995
Gene: KMT2A HGNC NCBI

Linked Data

ClinVar Variation Id: 1714682
ClinVar RCV Id: RCV002304391

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001184033.1:p.Phe2449Ser
CA6304392
NM_001197104.1:c.7346T>C