Canonical Allele Identifier: PA2828320464
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 497680

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356294.1:p.Thr1002Ile
CA224841749
NM_001369365.1:c.3005C>T