Canonical Allele Identifier: PA916010985
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 410408
ClinVar RCV Id: RCV002230405
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Ala40Ser
CA16611073
NM_001281492.2:c.118G>T