Canonical Allele Identifier: PA645295115
Gene: MYH11 HGNC NCBI

Linked Data

ClinVar Variation Id: 418581

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002465.1:p.Val1879Ile
CA7921178
NM_002474.3:c.5635G>A