Canonical Allele Identifier: PA2828319830
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 2188742
ClinVar RCV Id: RCV002620460

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356294.1:p.Gln482Glu
CA381935567
NM_001369365.1:c.1444C>G