Canonical Allele Identifier: PA658804586
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 517510

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000251.3:p.Met662Leu
CA6197657
NM_000260.4:c.1984A>T
CA381939227
NM_000260.4:c.1984A>C