Canonical Allele Identifier: PA658816259
Gene: MYH9 HGNC NCBI

Linked Data

ClinVar Variation Id: 504626
ClinVar RCV Id: RCV000610555 RCV000765636 RCV002531128
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002464.1:p.Val65Met
CA10210705
NM_002473.6:c.193G>A