Canonical Allele Identifier: PA2573223454
Gene: NGF HGNC NCBI

Linked Data

ClinVar Variation Id: 1517452
ClinVar RCV Id: RCV002027365
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002497.2:p.Thr177Ile
CA1022957
NM_002506.3:c.530C>T