Canonical Allele Identifier: PA2826826204
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 41755

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001280120.1:p.Ser498Phe
CA011660
NM_001293191.2:c.1493C>T