Canonical Allele Identifier: PA177015
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 164319
ClinVar RCV Id: RCV000151259 RCV000557182 RCV000788524
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Ala893Glu
CA012807
NM_000257.4:c.2678C>A