Canonical Allele Identifier: PA1139680450
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 964396

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120652.1:p.Arg1019Gln
CA224841770
NM_001127180.2:c.3056G>A