Canonical Allele Identifier: PA916002668
Gene: MYO16 HGNC NCBI

Linked Data

ClinVar Variation Id: 161689
ClinVar RCV Id: RCV000149225
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001185879.1:p.Leu1165Trp
CA174601
NM_001198950.3:c.3494T>G