Canonical Allele Identifier: PA345742
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 143212
ClinVar RCV Id: RCV000132751
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Arg1608Pro
CA015359
NM_000257.4:c.4823G>C