Canonical Allele Identifier: PA2826826776
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 492061
ClinVar RCV Id: RCV000581418

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001280121.1:p.Val150Gly
CA340134688
NM_001293192.2:c.449T>G