Canonical Allele Identifier: PA1139679849
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 862550

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120652.1:p.Phe632Cys
CA6197633
NM_001127180.2:c.1895T>G