Canonical Allele Identifier: PA2829995658
Gene: MYH11 HGNC NCBI

Linked Data

ClinVar Variation Id: 566668
ClinVar RCV Id: RCV000686542
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_074035.1:p.Pro673Ala
CA394868902
NM_022844.3:c.2017C>G