Canonical Allele Identifier: PA2825109029
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 2853260
ClinVar RCV Id: RCV003747713
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Arg249Pro
CA389052135
NM_000257.4:c.746G>C