Canonical Allele Identifier: PA916011702
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 89168
ClinVar RCV Id: RCV000074629 RCV000409637 RCV000487116 RCV000567227 RCV000701439 RCV003466931
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Arg59His
CA007978
NM_001281494.2:c.176G>A