Canonical Allele Identifier: PA2826631017
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1320382
ClinVar RCV Id: RCV001776361 RCV003759072
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Leu357Phe
CA346750614
NM_001281493.2:c.1069C>T