Canonical Allele Identifier: PA915957362
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 803009
ClinVar RCV Id: RCV000989187 RCV001183921 RCV002549722
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Arg1250Gly
CA389042770
NM_000257.4:c.3748C>G