Canonical Allele Identifier: PA278715
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 43340

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000251.3:p.Arg241His
CA278714
NM_000260.4:c.722G>A