Canonical Allele Identifier: PA132232
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 43168

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000251.3:p.Arg668Cys
CA132231
NM_000260.4:c.2002C>T