Canonical Allele Identifier: PA2829996929
Gene: MYH11 HGNC NCBI
ClinVar RCV:
RCV001938595
ClinVar Variation:
1417736
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_074035.1:p.Leu1257Pro
CA257128
NM_022844.3:c.3770T>C