Canonical Allele Identifier: PA658680113
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 483769
ClinVar RCV Id: RCV000573273 RCV001205595
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Ala84Thr
CA346735136
NM_000179.3:c.250G>A