Canonical Allele Identifier: PA2829995639
Gene: MYH11 HGNC NCBI

Linked Data

ClinVar Variation Id: 920067
ClinVar RCV Id: RCV001178618 RCV002483971
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_074035.1:p.Met665Val
CA394868958
NM_022844.3:c.1993A>G