Canonical Allele Identifier: PA338865
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 216310
ClinVar RCV Id: RCV000199786 RCV000215044 RCV001194335 RCV003996999 RCV003491941
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Arg1034Gln
CA070049
NM_000179.3:c.3101G>A