Canonical Allele Identifier: PA2829995567
Gene: MYH11 HGNC NCBI

Linked Data

ClinVar Variation Id: 3070695
ClinVar RCV Id: RCV004013205
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_074035.1:p.Asp623Val
CA394869233
NM_022844.3:c.1868A>T