Canonical Allele Identifier: PA2828319518
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 11851

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356294.1:p.Arg201Cys
CA277962
NM_001369365.1:c.601C>T