Canonical Allele Identifier: PA164969
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 141274
ClinVar RCV Id: RCV000129716 RCV000222346 RCV001089139 RCV003997519
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Thr1100Arg
CA012463
NM_000179.3:c.3299C>G