Canonical Allele Identifier: PA177089
Gene: MYH9 HGNC NCBI

Linked Data

ClinVar Variation Id: 164435
ClinVar RCV Id: RCV000151329 RCV000348717 RCV000293752 RCV000726552
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002464.1:p.Arg1466Trp
CA177087
NM_002473.6:c.4396C>T