Canonical Allele Identifier: PA916011733
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 89172
ClinVar RCV Id: RCV000074633 RCV000162441 RCV000202023 RCV000518839 RCV000524101 RCV001201190 RCV003162468 RCV003450922
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Leu68Ser
CA008059
NM_001281494.2:c.203T>C