Canonical Allele Identifier: PA2826630488
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 2433804
ClinVar RCV Id: RCV003132686

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Tyr236Phe
CA346747031
NM_001281493.2:c.707A>T