Canonical Allele Identifier: PA2825115579
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 2891552
ClinVar RCV Id: RCV003723011

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000251.3:p.Leu625Pro
CA381938467
NM_000260.4:c.1874T>C