Canonical Allele Identifier: PA2828321064
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 196935

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356294.1:p.Asn1537Ser
CA244758
NM_001369365.1:c.4610A>G