Canonical Allele Identifier: PA645480675
Gene: MYH3 HGNC NCBI

Linked Data

ClinVar Variation Id: 321708

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002461.2:p.Val1935Ala
CA10638885
NM_002470.4:c.5804T>C