Canonical Allele Identifier: PA2825432052
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 238338
ClinVar RCV Id: RCV000229901

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001041639.1:p.Lys464Asn
CA10581801
NM_001048174.1:c.1392G>C
CA340132460
NM_001048174.1:c.1392G>T