Canonical Allele Identifier: PA645294928
Gene: MYH9 HGNC NCBI

Linked Data

ClinVar Variation Id: 341536
ClinVar RCV Id: RCV000345258 RCV000378918 RCV003765978
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002464.1:p.Pro78Leu
CA10210700
NM_002473.6:c.233C>T