Canonical Allele Identifier: PA2825392321
Gene: MYH11 HGNC NCBI

Linked Data

ClinVar Variation Id: 3072191
ClinVar RCV Id: RCV004012221
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001035202.1:p.Ser648Gly
CA394869122
NM_001040113.2:c.1942A>G