Canonical Allele Identifier: PA645294931
Gene: MYH9 HGNC NCBI

Linked Data

ClinVar Variation Id: 341529
ClinVar RCV Id: RCV000319014 RCV000375903 RCV003727704
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002464.1:p.Asp384Asn
CA10210363
NM_002473.6:c.1150G>A