Canonical Allele Identifier: PA915957142
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 645070
ClinVar RCV Id: RCV000799087
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Ala998Pro
CA389046298
NM_000257.4:c.2992G>C