Canonical Allele Identifier: PA645295119
Gene: MYH11 HGNC NCBI

Linked Data

ClinVar Variation Id: 318089

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002465.1:p.Lys1925Arg
CA10647069
NM_002474.3:c.5774A>G