Canonical Allele Identifier: PA296777
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 181317
ClinVar RCV Id: RCV000158754
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Glu217Gln
CA016603
NM_000257.4:c.649G>C