Canonical Allele Identifier: PA2825085342
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 2013606
ClinVar RCV Id: RCV002834790
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Glu52Asp
CA346734952
NM_000179.3:c.156G>C
CA346734953
NM_000179.3:c.156G>T