Canonical Allele Identifier: PA2825627816
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 282113

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120652.1:p.Leu1916Val
CA6198859
NM_001127180.2:c.5746C>G