Canonical Allele Identifier: PA2826632922
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 89369
ClinVar RCV Id: RCV000074836 RCV000218926 RCV000223174 RCV000587747 RCV000524169 RCV000764431 RCV001358521 RCV003460680 RCV004019095 RCV004542742
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Thr798Met
CA012473
NM_001281493.2:c.2393C>T