Canonical Allele Identifier: PA1139672328
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 961527
ClinVar RCV Id: RCV001235235
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Val459Leu
CA389050757
NM_000257.4:c.1375G>C