Canonical Allele Identifier: PA294455
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 142597
ClinVar RCV Id: RCV000131804 RCV000225825 RCV000417386 RCV001355839 RCV003462024 RCV004544300
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Met492del
CA008666
NM_000179.3:c.1474_1476del