Canonical Allele Identifier: PA658747012
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 489991
ClinVar RCV Id: RCV000580164 RCV000695435 RCV003459430 RCV004001269
ClinVar Variation Id: 2567462
ClinVar RCV Id: RCV003311256 RCV003759810
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Thr906Ser
CA346755348
NM_000179.3:c.2716A>T
CA346755351
NM_000179.3:c.2717C>G