Canonical Allele Identifier: PA2499230350
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 1060806
ClinVar RCV Id: RCV001370283
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Leu1442Pro
CA389040090
NM_000257.4:c.4325T>C