Canonical Allele Identifier: PA645510094
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 438172

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000251.3:p.Ser617Pro
CA6197628
NM_000260.4:c.1849T>C