Canonical Allele Identifier: PA915959036
Gene: MYH11 HGNC NCBI

Linked Data

ClinVar Variation Id: 424073
ClinVar RCV Id: RCV000485735

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001035203.1:p.Ala1930Ser
CA16620073
NM_001040114.2:c.5788G>T