Canonical Allele Identifier: PA2825113082
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 2959858
ClinVar RCV Id: RCV003812033
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Arg1606Gly
CA389037575
NM_000257.4:c.4816C>G