Canonical Allele Identifier: PA658804593
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 497680

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000251.3:p.Thr1013Ile
CA224841749
NM_000260.4:c.3038C>T