Canonical Allele Identifier: PA1139675250
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 849036
ClinVar RCV Id: RCV001052917 RCV002339267 RCV003130127 RCV003532361
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Arg1662Cys
CA044615
NM_000257.4:c.4984C>T