Canonical Allele Identifier: PA2573192643
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1510838
ClinVar RCV Id: RCV002014164 RCV002458990 RCV003464388 RCV004011135
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Phe872Cys
CA346760212
NM_001281494.2:c.2615T>G