Canonical Allele Identifier: PA2826633844
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1719022
ClinVar RCV Id: RCV002296774
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Cys992Ser
CA346761374
NM_001281493.2:c.2974T>A
CA346761378
NM_001281493.2:c.2975G>C