Canonical Allele Identifier: PA658659172
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 454384
ClinVar RCV Id: RCV000542901 RCV000658395
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Arg1676Gln
CA389037108
NM_000257.4:c.5027G>A