Canonical Allele Identifier: PA916047301
Gene: MYO6 HGNC NCBI

Linked Data

ClinVar Variation Id: 505220
ClinVar RCV Id: RCV000607325
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001355794.1:p.Ile1224Thr
CA364762468
NM_001368865.1:c.3671T>C