Canonical Allele Identifier: PA915980673
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 438180

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120652.1:p.Arg241Cys
CA6197223
NM_001127180.2:c.721C>T