Canonical Allele Identifier: PA136017
Gene: MYO1A HGNC NCBI

Linked Data

ClinVar Variation Id: 8148

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005370.1:p.Val306Met
CA136016
NM_005379.3:c.916G>A