Canonical Allele Identifier: PA658805768
Gene: MYO1F HGNC NCBI

Linked Data

ClinVar Variation Id: 508620
ClinVar RCV Id: RCV000955029

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_036467.2:p.Asp954Tyr
CA9158739
NM_012335.4:c.2860G>T