Canonical Allele Identifier: PA2825393672
Gene: MYH11 HGNC NCBI

Linked Data

ClinVar Variation Id: 1468105
ClinVar RCV Id: RCV001970582 RCV004044639
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001035202.1:p.Ala1917Thr
CA7921156
NM_001040113.2:c.5749G>A