Canonical Allele Identifier: PA2826637392
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 89360
ClinVar RCV Id: RCV000131245 RCV000148653 RCV000212678 RCV000514075 RCV000764429 RCV001079820 RCV001262368 RCV003325179 RCV004537278
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Pro785Ser
CA012243
NM_001281494.2:c.2353C>T