Canonical Allele Identifier: PA306649
Gene: MYH11 HGNC NCBI
ClinVar RCV:
RCV000182548
ClinVar Variation:
201102
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001035202.1:p.Gly297Arg
CA306647
NM_001040113.2:c.889G>C
CA394869451
NM_001040113.2:c.889G>A