Canonical Allele Identifier: PA1139679900
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 813194
ClinVar RCV Id: RCV001199712

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120652.1:p.Arg666Pro
CA381939272
NM_001127180.2:c.1997G>C