Canonical Allele Identifier: PA2825112234
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 2712449
ClinVar RCV Id: RCV003586845
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Gln1098Glu
CA389044439
NM_000257.4:c.3292C>G