Canonical Allele Identifier: PA296684
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 181264
ClinVar RCV Id: RCV000158668 RCV000628917 RCV001185243 RCV002336357
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Ala1570Glu
CA015247
NM_000257.4:c.4709C>A