Canonical Allele Identifier: PA2573180502
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 1693020
ClinVar RCV Id: RCV002259447

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120652.1:p.Ile636Val
CA381938567
NM_001127180.2:c.1906A>G