Canonical Allele Identifier: PA2826631904
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 455210
ClinVar RCV Id: RCV000526734 RCV000567854 RCV004003680
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Val565Ile
CA069233
NM_001281493.2:c.1693G>A