Canonical Allele Identifier: PA658803358
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 229012

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120652.1:p.Arg1164Gln
CA6198071
NM_001127180.2:c.3491G>A