Canonical Allele Identifier: PA645417091
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 235032
ClinVar RCV Id: RCV000223810 RCV001187347 RCV001577895 RCV001854769 RCV002327098
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Glu1455Lys
CA10581171
NM_000257.4:c.4363G>A