Canonical Allele Identifier: PA645295120
Gene: MYH11 HGNC NCBI

Linked Data

ClinVar Variation Id: 419054
ClinVar RCV Id: RCV000486651 RCV001189159
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002465.1:p.Ala1963Thr
CA7921043
NM_002474.3:c.5887G>A