Canonical Allele Identifier: PA097639
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 42838
ClinVar RCV Id: RCV000201462 RCV000158800 RCV000195545 RCV000845295 RCV002381294
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Arg453His
CA010639
NM_000257.4:c.1358G>A