Canonical Allele Identifier: PA296586
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 181211
ClinVar RCV Id: RCV000158584 RCV001525776 RCV001850216 RCV003227682
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Glu1013Lys
CA013322
NM_000257.4:c.3037G>A