Canonical Allele Identifier: PA2826624887
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 410485
ClinVar RCV Id: RCV000507572 RCV002230119
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Ser112Thr
CA16610926
NM_001281492.2:c.335G>C