Canonical Allele Identifier: PA1139709163
Gene: NGF HGNC NCBI
ClinVar RCV:
RCV001052306
ClinVar Variation:
848531
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002497.2:p.Pro112His
CA1022991
NM_002506.3:c.335C>A