Canonical Allele Identifier: PA2826633518
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 89447
ClinVar RCV Id: RCV000167477 RCV001044651
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Val930Leu
CA013865
NM_001281493.2:c.2788G>C