Canonical Allele Identifier: PA645294939
Gene: MYH9 HGNC NCBI

Linked Data

ClinVar Variation Id: 341516

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002464.1:p.Arg1107Gln
CA10209689
NM_002473.6:c.3320G>A