Canonical Allele Identifier: PA1139673648
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 927446
ClinVar RCV Id: RCV001190753
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Lys994Thr
CA389046344
NM_000257.4:c.2981A>C