Canonical Allele Identifier: PA2825112513
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 2747535
ClinVar RCV Id: RCV003587639
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Arg1289Pro
CA389041777
NM_000257.4:c.3866G>C