Canonical Allele Identifier: PA2825430642
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 41759

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001041639.1:p.Pro4Leu
CA011771
NM_001048174.1:c.11C>T