Canonical Allele Identifier: PA2826829138
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 41755
ClinVar RCV Id: RCV000034672 RCV000119200 RCV000121601 RCV000132436 RCV001270289
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001280124.1:p.Ser487Phe
CA011660
NM_001293195.2:c.1460C>T