Canonical Allele Identifier: PA2573163693
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1435940
ClinVar RCV Id: RCV002001963
ClinVar Variation Id: 2587349
ClinVar RCV Id: RCV003360824
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Val801Leu
CA346753924
NM_000179.3:c.2401G>T
CA346753925
NM_000179.3:c.2401G>C