Canonical Allele Identifier: PA2826635463
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 185463
ClinVar RCV Id: RCV000164891 RCV000200231 RCV000480270 RCV000524126 RCV000781602 RCV001094683 RCV003462152 RCV004528912
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Glu337Lys
CA009445
NM_001281494.2:c.1009G>A