Canonical Allele Identifier: PA915998226
Gene: NGF HGNC NCBI

Linked Data

ClinVar Variation Id: 655197
ClinVar RCV Id: RCV000811327
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002497.2:p.Trp37Arg
CA1023066
NM_002506.3:c.109T>C
CA341837218
NM_002506.3:c.109T>A