Canonical Allele Identifier: PA2825627446
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 43278

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120652.1:p.Arg1705Trp
CA132381
NM_001127180.2:c.5113C>T