Canonical Allele Identifier: PA1139673505
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 945429
ClinVar RCV Id: RCV001216069 RCV002429921
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Cys905Tyr
CA389047298
NM_000257.4:c.2714G>A