Canonical Allele Identifier: PA645414721
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 235035
ClinVar RCV Id: RCV000223793 RCV000463441
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Thr265Asn
CA10581179
NM_000257.4:c.794C>A