Canonical Allele Identifier: PA1139683135
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 918380
ClinVar RCV Id: RCV001175948

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121897.1:p.Ser259Ala
CA340134773
NM_001128425.2:c.775T>G