Canonical Allele Identifier: PA338382
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 216323
ClinVar RCV Id: RCV000199066 RCV000214218 RCV000586061 RCV002267932 RCV003462324 RCV003491942 RCV003997003
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Arg300Gln
CA073560
NM_000179.3:c.899G>A