Canonical Allele Identifier: PA215830
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 41753

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121897.1:p.Arg426Cys
CA011618
NM_001128425.2:c.1276C>T