Canonical Allele Identifier: PA177113
Gene: MYH9 HGNC NCBI

Linked Data

ClinVar Variation Id: 164446
ClinVar RCV Id: RCV000151338 RCV000387348 RCV000293055 RCV000726812 RCV002243824
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002464.1:p.Ala958Thr
CA177111
NM_002473.6:c.2872G>A