Canonical Allele Identifier: PA2826627286
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 631116
ClinVar RCV Id: RCV000777165 RCV001320365 RCV001585704
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Lys674Thr
CA346753976
NM_001281492.2:c.2021A>C