Canonical Allele Identifier: PA2826631637
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 631116
ClinVar RCV Id: RCV000777165 RCV001320365 RCV001585704
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Lys502Thr
CA346753976
NM_001281493.2:c.1505A>C