Canonical Allele Identifier: PA2825394133
Gene: MYH11 HGNC NCBI

Linked Data

ClinVar Variation Id: 3071993
ClinVar RCV Id: RCV004012023

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001035203.1:p.Glu643Lys
CA394869153
NM_001040114.2:c.1927G>A