Canonical Allele Identifier: PA131739
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 42837
ClinVar RCV Id: RCV000035716
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Gln451Pro
CA010610
NM_000257.4:c.1352A>C