Canonical Allele Identifier: PA658654621
Gene: MYH9 HGNC NCBI

Linked Data

ClinVar Variation Id: 441002
ClinVar RCV Id: RCV000509305
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002464.1:p.Arg1855Trp
CA411372893
NM_002473.6:c.5563C>T