Canonical Allele Identifier: PA658660626
Gene: MYH11 HGNC NCBI

Linked Data

ClinVar Variation Id: 465711
ClinVar RCV Id: RCV000536873 RCV003528191
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001035202.1:p.Leu671Val
CA7922458
NM_001040113.2:c.2011C>G