Canonical Allele Identifier: PA2826625131
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 455357
ClinVar RCV Id: RCV000527690 RCV000575082 RCV003478111
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Lys169Asn
CA073549
NM_001281492.2:c.507G>T
CA346740697
NM_001281492.2:c.507G>C