Canonical Allele Identifier: PA105777
Gene: MYH3 HGNC NCBI

Linked Data

ClinVar Variation Id: 211557

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002461.2:p.Ser292Cys
CA209607
NM_002470.4:c.875C>G