Canonical Allele Identifier: PA2826634064
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 419915
ClinVar RCV Id: RCV000482748 RCV000491185 RCV000707566 RCV000986744 RCV003479136 RCV004003312 RCV004541518
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Arg1029Gln
CA16617720
NM_001281493.2:c.3086G>A