Canonical Allele Identifier: PA099299
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 43218

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000251.3:p.Arg1240Gln
CA278657
NM_000260.4:c.3719G>A