Canonical Allele Identifier: PA306648
Gene: MYH11 HGNC NCBI
ClinVar RCV:
RCV000182548
ClinVar Variation:
201102
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002465.1:p.Gly290Arg
CA306647
NM_002474.3:c.868G>C
CA394869451
NM_002474.3:c.868G>A