Canonical Allele Identifier: PA132401
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 43299

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000251.3:p.Gly1942Arg
CA132400
NM_000260.4:c.5824G>A
CA381954092
NM_000260.4:c.5824G>C