Canonical Allele Identifier: PA2825112005
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 3230903
ClinVar RCV Id: RCV004523017
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Cys947Tyr
CA389046865
NM_000257.4:c.2840G>A