Canonical Allele Identifier: PA105928
Gene: MYH9 HGNC NCBI

Linked Data

ClinVar Variation Id: 14078
ClinVar RCV Id: RCV000015129 RCV000523446 RCV000790354 RCV002490369 RCV003147289
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002464.1:p.Arg702Cys
CA257095
NM_002473.6:c.2104C>T