Canonical Allele Identifier: PA2826629784
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_001268422.1:p.Leu68Ser
CA008059
NM_001281493.2:c.203T>C