Canonical Allele Identifier: PA105936
Gene: MYH9 HGNC NCBI

Linked Data

ClinVar Variation Id: 14081
ClinVar RCV Id: RCV000015132 RCV000851738 RCV001851865
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002464.1:p.Arg702His
CA257101
NM_002473.6:c.2105G>A