Canonical Allele Identifier: PA2826625471
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 89173
ClinVar RCV Id: RCV000479933 RCV000569385 RCV000629837 RCV001290538 RCV001358106 RCV003997062
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Arg248Lys
CA008097
NM_001281492.2:c.743G>A
CA2838032275
NM_001281492.2:c.743_745delinsAAC