Canonical Allele Identifier: PA2825108995
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 2773968
ClinVar RCV Id: RCV003532730
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Asp239del
CA913184869
NM_000257.4:c.715_717del