Canonical Allele Identifier: PA2826636038
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1361030
ClinVar RCV Id: RCV001907319 RCV003164123
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Leu471Phe
CA346753179
NM_001281494.2:c.1411C>T