Canonical Allele Identifier: PA2826369496
Gene: MYO1A HGNC NCBI

Linked Data

ClinVar Variation Id: 164594

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001242970.1:p.Cys506Ser
CA177313
NM_001256041.2:c.1517G>C
CA385379273
NM_001256041.2:c.1516T>A