Canonical Allele Identifier: PA2829998618
Gene: MYH11 HGNC NCBI

Linked Data

ClinVar Variation Id: 2773782
ClinVar RCV Id: RCV003528097

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_074035.1:p.Asn1897Lys
CA394846793
NM_022844.3:c.5691C>G
CA394846794
NM_022844.3:c.5691C>A