Canonical Allele Identifier: PA188987
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 184444
ClinVar RCV Id: RCV000163700 RCV000480884 RCV000630065 RCV000662379 RCV002307420 RCV003462122 RCV003995273
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Thr764Asn
CA009966
NM_000179.3:c.2291C>A