Canonical Allele Identifier: PA105997
Gene: MYH9 HGNC NCBI

Linked Data

ClinVar Variation Id: 14073
ClinVar RCV Id: RCV000015119 RCV000790361 RCV001310800 RCV002466403
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002464.1:p.Glu1841Lys
CA257085
NM_002473.6:c.5521G>A