Canonical Allele Identifier: PA1139709327
Gene: NGF HGNC NCBI

Linked Data

ClinVar Variation Id: 933958
ClinVar RCV Id: RCV001202277
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002497.2:p.Arg221Leu
CA341836049
NM_002506.3:c.662G>T