Canonical Allele Identifier: PA2826626429
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 141265
ClinVar RCV Id: RCV000129705 RCV000200701 RCV000587763 RCV000708871 RCV000765684
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Thr475Ser
CA009251
NM_001281492.2:c.1424C>G
CA346749406
NM_001281492.2:c.1423A>T