Canonical Allele Identifier: PA2826629751
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1350133
ClinVar RCV Id: RCV002039524
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Pro60Ala
CA346741811
NM_001281493.2:c.178C>G