Canonical Allele Identifier: PA351838
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 222720
ClinVar RCV Id: RCV000208181
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Glu179Ala
CA351836
NM_000257.4:c.536A>C