Canonical Allele Identifier: PA2825627470
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 1309834
ClinVar RCV Id: RCV001756902

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120652.1:p.Pro1713Thr
CA381952249
NM_001127180.2:c.5137C>A