Canonical Allele Identifier: PA2825432022
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 967721
ClinVar Variation Id: 2567648
ClinVar RCV Id: RCV003278609

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001041639.1:p.Thr455Ser
CA340132548
NM_001048174.1:c.1364C>G
CA340132551
NM_001048174.1:c.1363A>T