Canonical Allele Identifier: PA916011374
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 237185
ClinVar RCV Id: RCV000225977 RCV000662750 RCV000480996 RCV000584577
ClinVar Variation Id: 1318812
ClinVar RCV Id: RCV001753359 RCV001868751
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Met944Leu
CA10582083
NM_001281492.2:c.2830A>T
CA346757976
NM_001281492.2:c.2830A>C