Canonical Allele Identifier: PA2825112605
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 1714334
ClinVar RCV Id: RCV002297280
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Glu1349Gly
CA389041118
NM_000257.4:c.4046A>G