Canonical Allele Identifier: PA2825112991
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 1929446
ClinVar RCV Id: RCV002635364
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Leu1551Pro
CA389037929
NM_000257.4:c.4652T>C