Canonical Allele Identifier: PA2826629557
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 823308
ClinVar RCV Id: RCV001019445 RCV003594078
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Lys15Asn
CA346740832
NM_001281493.2:c.45G>C
CA346740835
NM_001281493.2:c.45G>T