Canonical Allele Identifier: PA2573165238
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 1511366
ClinVar RCV Id: RCV002016667
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Glu1886Val
CA389034754
NM_000257.4:c.5657A>T