Canonical Allele Identifier: PA2828321818
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 43338

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356294.1:p.Gly2165Ser
CA132445
NM_001369365.1:c.6493G>A