Canonical Allele Identifier: PA212711
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 164316
ClinVar RCV Id: RCV000208124 RCV000240635 RCV000685493 RCV001537865 RCV002426717
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Arg904Cys
CA012904
NM_000257.4:c.2710C>T