Canonical Allele Identifier: PA915958486
Gene: MYH11 HGNC NCBI

Linked Data

ClinVar Variation Id: 618737
ClinVar RCV Id: RCV000757518
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001035203.1:p.Arg693Thr
CA394868724
NM_001040114.2:c.2078G>C