Canonical Allele Identifier: PA2826634051
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 410491
ClinVar RCV Id: RCV000775745 RCV000466998 RCV001555679 RCV003470467 RCV004001844
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Leu1028Val
CA16610987
NM_001281493.2:c.3082C>G