Canonical Allele Identifier: PA2573165109
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 1477453
ClinVar RCV Id: RCV002018746
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Leu1100Arg
CA389044411
NM_000257.4:c.3299T>G