Canonical Allele Identifier: PA094272
Gene: MLH3 HGNC NCBI
ClinVar Allele:
20598
ClinVar RCV:
RCV000005898
ClinVar Variation:
5559
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001035197.1:p.Asn499Ser
CA117590
NM_001040108.1:c.1496A>G