Canonical Allele Identifier: PA645294961
Gene: MYH9 HGNC NCBI

Linked Data

ClinVar Variation Id: 341494
ClinVar RCV Id: RCV000368697 RCV000394413 RCV000787013 RCV001590995 RCV002523218
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002464.1:p.Leu1819Arg
CA10209055
NM_002473.6:c.5456T>G