Canonical Allele Identifier: PA645417801
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 291305
ClinVar RCV Id: RCV000296105
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Ile1724del
CA10607095
NM_000257.4:c.5171_5173del