Canonical Allele Identifier: PA2825432124
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 41755

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001041639.1:p.Ser487Phe
CA011660
NM_001048174.1:c.1460C>T