Canonical Allele Identifier: PA2826632854
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 525751

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Pro784Ser
CA346758131
NM_001281493.2:c.2350C>T