Canonical Allele Identifier: PA2825113069
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 3069632
ClinVar RCV Id: RCV004008176
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Leu1601Val
CA389037606
NM_000257.4:c.4801C>G