Canonical Allele Identifier: PA2580147842
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 2147174
ClinVar RCV Id: RCV003077055

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120652.1:p.Ile1171Met
CA381946839
NM_001127180.2:c.3513C>G