Canonical Allele Identifier: PA2828319868
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 164672

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356294.1:p.Leu517Arg
CA177372
NM_001369365.1:c.1550T>G