Canonical Allele Identifier: PA2825393666
Gene: MYH11 HGNC NCBI

Linked Data

ClinVar Variation Id: 927693
ClinVar RCV Id: RCV001191153 RCV001240359 RCV002484046
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001035202.1:p.Arg1912Gln
CA394846654
NM_001040113.2:c.5735G>A