Canonical Allele Identifier: PA2573064562
Gene: MYH11 HGNC NCBI

Linked Data

ClinVar Variation Id: 1332580
ClinVar RCV Id: RCV001805626 RCV001869553
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001035202.1:p.Pro1940Ser
CA7921108
NM_001040113.2:c.5818C>T