Canonical Allele Identifier: PA891844973
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 567504
ClinVar RCV Id: RCV000687609
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Gly1556Asp
CA389037896
NM_000257.4:c.4667G>A