Canonical Allele Identifier: PA2828285379
Gene: MYO6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1699715
ClinVar RCV Id: RCV002273572
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001355066.1:p.Trp1180Arg
CA364761973
NM_001368137.1:c.3538T>C
CA364761975
NM_001368137.1:c.3538T>A