Canonical Allele Identifier: PA645382517
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 231236
ClinVar RCV Id: RCV000222312 RCV000507745 RCV000818639 RCV002478792 RCV002508928 RCV003462456
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Val890Phe
CA10578112
NM_000179.3:c.2668G>T