Canonical Allele Identifier: PA2826625111
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 2119554
ClinVar RCV Id: RCV003054714
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Lys165Asn
CA346740674
NM_001281492.2:c.495A>C
CA346740675
NM_001281492.2:c.495A>T