Canonical Allele Identifier: PA645294933
Gene: MYH9 HGNC NCBI

Linked Data

ClinVar Variation Id: 378216
ClinVar RCV Id: RCV000425185 RCV001145336 RCV001145337
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002464.1:p.Gly681Ser
CA10210100
NM_002473.6:c.2041G>A