Canonical Allele Identifier: PA658660694
Gene: MYH11 HGNC NCBI

Linked Data

ClinVar Variation Id: 465724
ClinVar RCV Id: RCV000559707 RCV002497126 RCV003302831
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001035202.1:p.Leu1134Val
CA394861996
NM_001040113.2:c.3400C>G