Canonical Allele Identifier: PA097626
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 14102
ClinVar RCV Id: RCV000158787 RCV000015158 RCV001170740 RCV000456661 RCV000515361 RCV000621657
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Arg403Trp
CA010360
NM_000257.4:c.1207C>T