Canonical Allele Identifier: PA099679
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 43295

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000251.3:p.Pro1887Leu
CA278690
NM_000260.4:c.5660C>T