Canonical Allele Identifier: PA1139675954
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 918474
ClinVar RCV Id: RCV001176108 RCV001875797
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Phe1896Cys
CA389034686
NM_000257.4:c.5687T>G