Canonical Allele Identifier: PA2825627220
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 306189

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120652.1:p.Asn1576Lys
CA10639467
NM_001127180.2:c.4728C>A
CA381951047
NM_001127180.2:c.4728C>G