Canonical Allele Identifier: PA2825431922
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 1057542
ClinVar RCV Id: RCV001366548

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001041639.1:p.Ile421Val
CA340132765
NM_001048174.1:c.1261A>G