Canonical Allele Identifier: PA2825432184
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_001041639.1:p.Phe504Leu
CA057021
NM_001048174.1:c.1512C>A
CA340131641
NM_001048174.1:c.1512C>G
CA340131650
NM_001048174.1:c.1510T>C