Canonical Allele Identifier: PA2826854645
Gene: MYO6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1310791
ClinVar RCV Id: RCV001767905

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001287828.1:p.His1173Asp
CA364762042
NM_001300899.2:c.3517C>G