Canonical Allele Identifier: PA2826630145
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 2676816
ClinVar RCV Id: RCV003461948
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Trp154Cys
CA346744884
NM_001281493.2:c.462G>C
CA346744888
NM_001281493.2:c.462G>T