Canonical Allele Identifier: PA2827151699
Gene: NRG1 HGNC NCBI

Linked Data

ClinVar Variation Id: 218702
ClinVar RCV Id: RCV000202884
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001309135.1:p.Val133Leu
CA249080
NM_001322206.2:c.397G>C
CA370923274
NM_001322206.2:c.397G>T