Canonical Allele Identifier: PA2829397853
Gene: MYH11 HGNC NCBI

Linked Data

ClinVar Variation Id: 2433870
ClinVar RCV Id: RCV003132734
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002465.1:p.Ala1414Glu
CA2580090856
NM_002474.3:c.4241_4242delinsAG