Canonical Allele Identifier: PA891859371
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_001035202.1:p.Pro680Ala
CA394868902
NM_001040113.2:c.2038C>G