Canonical Allele Identifier: PA177314
Gene: MYO1A HGNC NCBI

Linked Data

ClinVar Variation Id: 164594

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005370.1:p.Cys506Ser
CA177313
NM_005379.3:c.1517G>C
CA385379273
NM_005379.3:c.1516T>A