Canonical Allele Identifier: PA658746089
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 489978
ClinVar RCV Id: RCV000579661
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Ser702Pro
CA346750915
NM_000179.3:c.2104T>C