Canonical Allele Identifier: PA658816247
Gene: MYH9 HGNC NCBI

Linked Data

ClinVar Variation Id: 505004
ClinVar RCV Id: RCV000613702 RCV001540673 RCV004527680 RCV004024891
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002464.1:p.Gln4Arg
CA10210742
NM_002473.6:c.11A>G