Canonical Allele Identifier: PA136007
Gene: MYO1A HGNC NCBI

Linked Data

ClinVar Variation Id: 45309
ClinVar RCV Id: RCV000038473

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005370.1:p.Arg768Trp
CA136006
NM_005379.3:c.2302C>T