Canonical Allele Identifier: PA658659170
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 451858
ClinVar RCV Id: RCV000522797 RCV002341228 RCV004003633
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Ile1673Val
CA044805
NM_000257.4:c.5017A>G