Canonical Allele Identifier: PA097637
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 14089
ClinVar RCV Id: RCV000015145 RCV000035717 RCV000158799 RCV000230258 RCV000618958 RCV001170514 RCV001375645 RCV004532356
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Arg453Cys
CA010630
NM_000257.4:c.1357C>T