Canonical Allele Identifier: PA658654042
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 229012

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000251.3:p.Arg1164Gln
CA6198071
NM_000260.4:c.3491G>A