Canonical Allele Identifier: PA106046
Gene: MYH9 HGNC NCBI

Linked Data

ClinVar Variation Id: 14083
ClinVar RCV Id: RCV000015138 RCV000477821 RCV000790352 RCV001537286
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002464.1:p.Ser96Leu
CA257103
NM_002473.6:c.287C>T