Canonical Allele Identifier: PA177098
Gene: MYH9 HGNC NCBI

Linked Data

ClinVar Variation Id: 164438
ClinVar RCV Id: RCV000151332 RCV000276612 RCV000331644 RCV001850062
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002464.1:p.Arg1433Cys
CA177096
NM_002473.6:c.4297C>T