Canonical Allele Identifier: PA2826830372
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 231635
ClinVar RCV Id: RCV001582750 RCV000221052 RCV000476152
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001280125.1:p.Phe412Leu
CA057021
NM_001293196.2:c.1236C>A
CA340131641
NM_001293196.2:c.1236C>G
CA340131650
NM_001293196.2:c.1234T>C