Canonical Allele Identifier: PA658820477
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_004990.3:p.Ile1215Thr
CA364762468
NM_004999.4:c.3644T>C