Canonical Allele Identifier: PA658815767
Gene: MYH3 HGNC NCBI

Linked Data

ClinVar Variation Id: 522656
ClinVar RCV Id: RCV000625795

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002461.2:p.Arg1609Lys
CA398136862
NM_002470.4:c.4826G>A