Canonical Allele Identifier: PA2828319472
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 43264

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356294.1:p.Thr154Met
CA278676
NM_001369365.1:c.461C>T