Canonical Allele Identifier: PA645427375
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 306185

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000251.3:p.Arg1347Cys
CA6198300
NM_000260.4:c.4039C>T