Canonical Allele Identifier: PA913192046
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 632905

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Pro12Leu
CA46687631
NM_000179.3:c.35C>T