Canonical Allele Identifier: PA1139673870
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 925499
ClinVar RCV Id: RCV001187475 RCV002505788
ClinVar Variation Id: 959570
ClinVar RCV Id: RCV001232948 RCV001547746 RCV003532911
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Gln1098His
CA036679
NM_000257.4:c.3294G>C
CA257816448
NM_000257.4:c.3294G>T