Canonical Allele Identifier: PA658816318
Gene: MYH9 HGNC NCBI

Linked Data

ClinVar Variation Id: 523453

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002464.1:p.Asp1424Gly
CA323590385
NM_002473.6:c.4271A>G