Canonical Allele Identifier: PA2828320006
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 1326431
ClinVar RCV Id: RCV001786611

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356294.1:p.Ala616Thr
CA381938481
NM_001369365.1:c.1846G>A