Canonical Allele Identifier: PA132300
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 43215

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000251.3:p.Cys1201Ser
CA132299
NM_000260.4:c.3602G>C
CA381947024
NM_000260.4:c.3601T>A