Canonical Allele Identifier: PA2826632420
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 186981
ClinVar RCV Id: RCV000166654 RCV000198691 RCV000214752 RCV000662610 RCV000767216 RCV000764425
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Thr685Ala
CA011202
NM_001281493.2:c.2053A>G