Canonical Allele Identifier: PA2573223429
Gene: NGF HGNC NCBI

Linked Data

ClinVar Variation Id: 1403014
ClinVar RCV Id: RCV001925260 RCV003989134
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002497.2:p.Arg121Trp
CA341836718
NM_002506.3:c.361C>T