Canonical Allele Identifier: PA2826627279
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 491896
ClinVar RCV Id: RCV000582673 RCV000629957
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Pro672Ser
CA346753942
NM_001281492.2:c.2014C>T