Canonical Allele Identifier: PA2829399135
Gene: MYH11 HGNC NCBI

Linked Data

ClinVar Variation Id: 3073302
ClinVar RCV Id: RCV004015316
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002465.1:p.Ala1910Val
CA394846542
NM_002474.3:c.5729C>T