Canonical Allele Identifier: PA645294927
Gene: MYH9 HGNC NCBI

Linked Data

ClinVar Variation Id: 377017
ClinVar RCV Id: RCV000424167 RCV000790339
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002464.1:p.Phe41Ser
CA16603232
NM_002473.6:c.122T>C