Canonical Allele Identifier: PA097730
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 14104
ClinVar RCV Id: RCV000158512 RCV000241836 RCV000758071 RCV001170501 RCV001194067 RCV001594372 RCV002496366 RCV000015160
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Arg719Trp
CA011779
NM_000257.4:c.2155C>T