Canonical Allele Identifier: PA2825432162
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 127833
ClinVar Variation Id: 492024

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001041639.1:p.Met496Leu
CA011670
NM_001048174.1:c.1486A>T
CA340131758
NM_001048174.1:c.1486A>C