Canonical Allele Identifier: PA2829399117
Gene: MYH11 HGNC NCBI

Linked Data

ClinVar Variation Id: 927693
ClinVar RCV Id: RCV001191153 RCV001240359 RCV002484046
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002465.1:p.Arg1905Gln
CA394846654
NM_002474.3:c.5714G>A