Canonical Allele Identifier: PA212693
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 42965
ClinVar RCV Id: RCV000158611 RCV000627139 RCV001059046 RCV001449662 RCV003485529
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Arg1193His
CA013815
NM_000257.4:c.3578G>A