Canonical Allele Identifier: PA105705
Gene: MYH3 HGNC NCBI

Linked Data

ClinVar Variation Id: 14138

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002461.2:p.Arg672His
CA123755
NM_002470.4:c.2015G>A