Canonical Allele Identifier: PA2826633591
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 231746
ClinVar RCV Id: RCV000219285 RCV000629717 RCV001193097 RCV001565850 RCV003997923
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Leu942del
CA10578157
NM_001281493.2:c.2826_2828del