Canonical Allele Identifier: PA2825115221
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 3007060
ClinVar RCV Id: RCV003868699

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000251.3:p.Ile507Met
CA381935731
NM_000260.4:c.1521C>G