Canonical Allele Identifier: PA177101
Gene: MYH9 HGNC NCBI

Linked Data

ClinVar Variation Id: 164439
ClinVar RCV Id: RCV000151333 RCV000291994 RCV000386272 RCV000724779
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002464.1:p.Asp1409Asn
CA177099
NM_002473.6:c.4225G>A