Canonical Allele Identifier: PA2829395790
Gene: MYH11 HGNC NCBI

Linked Data

ClinVar Variation Id: 1466820
ClinVar RCV Id: RCV001966180
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002465.1:p.Ser641Arg
CA394869116
NM_002474.3:c.1923C>A
CA394869117
NM_002474.3:c.1923C>G
CA394869123
NM_002474.3:c.1921A>C