Canonical Allele Identifier: PA916010989
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 89180
ClinVar RCV Id: RCV000131942 RCV000422207 RCV000524105 RCV000410444 RCV001354476 RCV001719808 RCV003149716 RCV004542739
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Pro42Ser
CA008371
NM_001281492.2:c.124C>T