Canonical Allele Identifier: PA658671607
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 485900
ClinVar RCV Id: RCV000573959 RCV001051371
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121897.1:p.Met121Val
CA340136286
NM_001128425.2:c.361A>G