Canonical Allele Identifier: PA2829998613
Gene: MYH11 HGNC NCBI

Linked Data

ClinVar Variation Id: 920793
ClinVar RCV Id: RCV001179762

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_074035.1:p.Arg1895Ser
CA394846832
NM_022844.3:c.5683C>A