Canonical Allele Identifier: PA2826631126
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 2707953
ClinVar RCV Id: RCV003595039

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Ser380Ala
CA346750749
NM_001281493.2:c.1138T>G