Canonical Allele Identifier: PA913194212
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 629776
ClinVar RCV Id: RCV000774488 RCV001575007 RCV001856089 RCV004535903
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Arg1141Gln
CA389043939
NM_000257.4:c.3422G>A