Canonical Allele Identifier: PA2580273511
Gene: MYH3 HGNC NCBI

Linked Data

ClinVar Variation Id: 2293655
ClinVar RCV Id: RCV002841700

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002461.2:p.Asp956Ala
CA398156935
NM_002470.4:c.2867A>C