Canonical Allele Identifier: PA658680117
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 480918
ClinVar RCV Id: RCV000572033 RCV000629809 RCV001566523 RCV003316740 RCV003465183 RCV002265801
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Thr86Ile
CA46688635
NM_000179.3:c.257C>T