Canonical Allele Identifier: PA2825427892
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 480000

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001041637.1:p.Glu161Asp
CA340135574
NM_001048172.1:c.483G>C
CA340135578
NM_001048172.1:c.483G>T