Canonical Allele Identifier: PA658659163
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 454382
ClinVar RCV Id: RCV000525541
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Gln1656Glu
CA389037233
NM_000257.4:c.4966C>G