Canonical Allele Identifier: PA658680346
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 479949
ClinVar RCV Id: RCV000561282 RCV003767109
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Ser292Thr
CA346740653
NM_000179.3:c.875G>C