Canonical Allele Identifier: PA2829399083
Gene: MYH11 HGNC NCBI

Linked Data

ClinVar Variation Id: 3074525
ClinVar RCV Id: RCV004014059
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002465.1:p.Arg1884Lys
CA7921175
NM_002474.3:c.5651G>A