Canonical Allele Identifier: PA097975
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 577406
ClinVar RCV Id: RCV000700152
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Asp953His
CA389046802
NM_000257.4:c.2857G>C