Canonical Allele Identifier: PA184335
Gene: MYH9 HGNC NCBI

Linked Data

ClinVar Variation Id: 179392
ClinVar RCV Id: RCV000156181 RCV001785481 RCV004544449
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002464.1:p.Arg1703Trp
CA184333
NM_002473.6:c.5107C>T