Canonical Allele Identifier: PA915980909
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 242392

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120652.1:p.Arg657Trp
CA16616838
NM_001127180.2:c.1969C>T