Canonical Allele Identifier: PA2826633550
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 188261
ClinVar RCV Id: RCV001020953 RCV001373676 RCV003995614
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Glu935Asp
CA013945
NM_001281493.2:c.2805G>C
CA346761001
NM_001281493.2:c.2805G>T