Canonical Allele Identifier: PA296790
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 181325
ClinVar RCV Id: RCV000505791 RCV002516389
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Ala259Glu
CA016814
NM_000257.4:c.776C>A