Canonical Allele Identifier: PA294116
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 141299
ClinVar RCV Id: RCV000129766 RCV000409325 RCV000464994 RCV000515187 RCV000586138 RCV001175358 RCV003153418 RCV003467119 RCV003997523
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Pro1082Ser
CA012124
NM_000179.3:c.3244C>T