Canonical Allele Identifier: PA658816330
Gene: MYH9 HGNC NCBI

Linked Data

ClinVar Variation Id: 523083
ClinVar RCV Id: RCV000626302

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002464.1:p.Lys1585del
CA10209303
NM_002473.6:c.4753_4755del