Canonical Allele Identifier: PA915956730
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 640102
ClinVar RCV Id: RCV000793056
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Thr446Ile
CA389050836
NM_000257.4:c.1337C>T