Canonical Allele Identifier: PA186269
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 89172
ClinVar RCV Id: RCV000074633 RCV000162441 RCV000202023 RCV000518839 RCV000524101 RCV001201190 RCV003162468 RCV003450922
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Leu370Ser
CA008059
NM_000179.3:c.1109T>C