Canonical Allele Identifier: PA345835
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 155812
ClinVar RCV Id: RCV000143920
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Tyr287Cys
CA016907
NM_000257.4:c.860A>G