Canonical Allele Identifier: PA916011512
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 644510
ClinVar RCV Id: RCV000798446 RCV002458443 RCV002271586 RCV003442082
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Glu991Asp
CA070730
NM_001281492.2:c.2973G>C
CA346758783
NM_001281492.2:c.2973G>T