Canonical Allele Identifier: PA645294952
Gene: MYH9 HGNC NCBI

Linked Data

ClinVar Variation Id: 341501
ClinVar RCV Id: RCV000308851 RCV000405444 RCV001355046
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002464.1:p.Arg1464His
CA10209369
NM_002473.6:c.4391G>A