Canonical Allele Identifier: PA2825627793
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 43298

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120652.1:p.Leu1897Pro
CA278691
NM_001127180.2:c.5690T>C