Canonical Allele Identifier: PA163502
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 89186
ClinVar RCV Id: RCV000128873 RCV000791437 RCV000214282 RCV002288560 RCV003460660
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Leu435Pro
CA008468
NM_000179.3:c.1304T>C