Canonical Allele Identifier: PA099334
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 43278

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000251.3:p.Arg1743Trp
CA132381
NM_000260.4:c.5227C>T