Canonical Allele Identifier: PA645427714
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 228282
ClinVar Variation Id: 2695558
ClinVar RCV Id: RCV003542162

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000251.3:p.Lys2021Arg
CA10576905
NM_000260.4:c.6062A>G
CA2697548854
NM_000260.4:c.6062_6063delinsGA