Canonical Allele Identifier: PA2829998700
Gene: MYH11 HGNC NCBI

Linked Data

ClinVar Variation Id: 374963
ClinVar RCV Id: RCV000415719 RCV000772071 RCV001555668 RCV001374827
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_074035.1:p.Thr1911Met
CA7921155
NM_022844.3:c.5732C>T