Canonical Allele Identifier: PA916018661
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 41759

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001280124.1:p.Pro4Leu
CA011771
NM_001293195.2:c.11C>T