Canonical Allele Identifier: PA2825112816
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 2051795
ClinVar RCV Id: RCV002927525
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Gln1458Glu
CA042063
NM_000257.4:c.4372C>G