Canonical Allele Identifier: PA915965111
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 651137
ClinVar RCV Id: RCV000806430 RCV003353039
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Val828Leu
CA346754178
NM_000179.3:c.2482G>C