Canonical Allele Identifier: PA658802002
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 525666
ClinVar RCV Id: RCV000629838 RCV002385975
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Thr327Pro
CA346741012
NM_000179.3:c.979A>C