Canonical Allele Identifier: PA645294936
Gene: MYH9 HGNC NCBI
ClinVar Allele:
29123
ClinVar RCV:
RCV000015139
ClinVar Variation:
14084
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002464.1:p.Gln1068_Leu1074del
CA2695230755
NM_002473.6:c.3202_3222del