Canonical Allele Identifier: PA645414681
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 312917
ClinVar RCV Id: RCV000319627 RCV000355709 RCV000359186 RCV000392518 RCV001094229 RCV001525479 RCV003320177
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Ile220Leu
CA10644000
NM_000257.4:c.658A>C