Canonical Allele Identifier: PA2825091222
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 644510
ClinVar RCV Id: RCV000798446 RCV002458443 RCV002271586 RCV003442082
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Glu1121Asp
CA070730
NM_000179.3:c.3363G>C
CA346758783
NM_000179.3:c.3363G>T