Canonical Allele Identifier: PA2828320035
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 229000

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356294.1:p.Arg638Trp
CA6197652
NM_001369365.1:c.1912C>T