Canonical Allele Identifier: PA645408013
Gene: MYH11 HGNC NCBI

Linked Data

ClinVar Variation Id: 318091
ClinVar RCV Id: RCV000268264 RCV000360574 RCV001119049
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001035202.1:p.Val1928Met
CA10643049
NM_001040113.2:c.5782G>A