Canonical Allele Identifier: PA2826634230
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1766191
ClinVar RCV Id: RCV002371249
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Asn5Thr
CA346740737
NM_001281494.2:c.14A>C