Canonical Allele Identifier: PA2829995640
Gene: MYH11 HGNC NCBI

Linked Data

ClinVar Variation Id: 2716691
ClinVar RCV Id: RCV003513902
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_074035.1:p.Met665Ile
CA394868951
NM_022844.3:c.1995G>A
CA394868952
NM_022844.3:c.1995G>C
CA394868953
NM_022844.3:c.1995G>T