Canonical Allele Identifier: PA2828320061
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 983065
ClinVar RCV Id: RCV001262911

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356294.1:p.Arg657Leu
CA381939293
NM_001369365.1:c.1970G>T