Canonical Allele Identifier: PA2826630107
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 935156
ClinVar RCV Id: RCV001203684 RCV002379769 RCV004010631
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Glu144Lys
CA346744558
NM_001281493.2:c.430G>A