Canonical Allele Identifier: PA645408016
Gene: MYH11 HGNC NCBI

Linked Data

ClinVar Variation Id: 318089
ClinVar RCV Id: RCV000309241 RCV000366285 RCV001119048
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001035202.1:p.Lys1932Arg
CA10647069
NM_001040113.2:c.5795A>G