Canonical Allele Identifier: PA105964
Gene: MYH9 HGNC NCBI

Linked Data

ClinVar Variation Id: 14082
ClinVar RCV Id: RCV000015134 RCV000790358 RCV001271110 RCV002496364 RCV002513058 RCV002466404
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002464.1:p.Asp1424Asn
CA123739
NM_002473.6:c.4270G>A