Canonical Allele Identifier: PA658804408
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 506187
ClinVar RCV Id: RCV004017695
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Ile285Thr
CA389051898
NM_000257.4:c.854T>C