Canonical Allele Identifier: PA2826626668
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1320382
ClinVar RCV Id: RCV001776361 RCV003759072
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Leu529Phe
CA346750614
NM_001281492.2:c.1585C>T