Canonical Allele Identifier: PA2573165188
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 1348793
ClinVar RCV Id: RCV002046609
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Leu1657Pro
CA389037224
NM_000257.4:c.4970T>C