Canonical Allele Identifier: PA211692
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_000170.1:p.Pro1087Ser
CA012243
NM_000179.3:c.3259C>T