Canonical Allele Identifier: PA296795
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 181328
ClinVar RCV Id: RCV000158770
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Ser291Pro
CA016911
NM_000257.4:c.871T>C