Canonical Allele Identifier: PA2825109738
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 2866884
ClinVar RCV Id: RCV003747950
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Tyr410His
CA389051080
NM_000257.4:c.1228T>C