Canonical Allele Identifier: PA1139679803
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 813193
ClinVar RCV Id: RCV001199711

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120652.1:p.Leu618Arg
CA381938404
NM_001127180.2:c.1853T>G