Canonical Allele Identifier: PA658655587
Gene: MYH11 HGNC NCBI

Linked Data

ClinVar Variation Id: 138358
ClinVar RCV Id: RCV000126968 RCV000475215 RCV000776051 RCV001311430
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001035203.1:p.Glu1899Asp
CA292332
NM_001040114.2:c.5697G>C
CA394846869
NM_001040114.2:c.5697G>T