Canonical Allele Identifier: PA2825116279
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 964396

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000251.3:p.Arg1019Gln
CA224841770
NM_000260.4:c.3056G>A