Canonical Allele Identifier: PA2827558592
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 2676891
ClinVar RCV Id: RCV003463071

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001337580.1:p.Phe338Leu
CA340132566
NM_001350651.2:c.1014T>G
CA340132568
NM_001350651.2:c.1014T>A
CA340132577
NM_001350651.2:c.1012T>C