Canonical Allele Identifier: PA2825109899
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 3062303
ClinVar RCV Id: RCV003986025
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Ile457Lys
CA389050767
NM_000257.4:c.1370T>A