Canonical Allele Identifier: PA099655
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 11856

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000251.3:p.Met599Ile
CA121721
NM_000260.4:c.1797G>A
CA381937289
NM_000260.4:c.1797G>T
CA381937291
NM_000260.4:c.1797G>C