Canonical Allele Identifier: PA2826635490
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 647393
ClinVar Variation Id: 1497615

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Lys344Asn
CA346750442
NM_001281494.2:c.1032G>C
CA346750445
NM_001281494.2:c.1032G>T