Canonical Allele Identifier: PA2828320608
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 229012

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356294.1:p.Arg1153Gln
CA6198071
NM_001369365.1:c.3458G>A