Canonical Allele Identifier: PA2826854652
Gene: MYO6 HGNC NCBI

Linked Data

ClinVar Variation Id: 505220
ClinVar RCV Id: RCV000607325

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001287828.1:p.Ile1192Thr
CA364762468
NM_001300899.2:c.3575T>C