Canonical Allele Identifier: PA136001
Gene: MYO1A HGNC NCBI

Linked Data

ClinVar Variation Id: 45307

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005370.1:p.Pro426Leu
CA136000
NM_005379.3:c.1277C>T