Canonical Allele Identifier: PA168926
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 89180
ClinVar RCV Id: RCV000131942 RCV000422207 RCV000524105 RCV000410444 RCV001354476 RCV001719808 RCV003149716 RCV004542739
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Pro42Ser
CA008371
NM_000179.3:c.124C>T