Canonical Allele Identifier: PA2826631112
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 2587334
ClinVar RCV Id: RCV003360812
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Leu377Phe
CA346750735
NM_001281493.2:c.1131G>C
CA346750736
NM_001281493.2:c.1131G>T