Canonical Allele Identifier: PA2825113057
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 1996661
ClinVar RCV Id: RCV002823794
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Val1594Met
CA389037647
NM_000257.4:c.4780G>A