Canonical Allele Identifier: PA1139671746
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 854576
ClinVar RCV Id: RCV001059657
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Gln219Glu
CA389052321
NM_000257.4:c.655C>G