Canonical Allele Identifier: PA645294943
Gene: MYH9 HGNC NCBI

Linked Data

ClinVar Variation Id: 341511
ClinVar RCV Id: RCV000271817 RCV000326885 RCV002480197 RCV002523221
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002464.1:p.Arg1226Gln
CA10209593
NM_002473.6:c.3677G>A