Canonical Allele Identifier: PA2825112651
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 2433935
ClinVar RCV Id: RCV003131646
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Lys1391Arg
CA389040625
NM_000257.4:c.4172A>G