Canonical Allele Identifier: PA2826912699
Gene: FN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1369933
ClinVar RCV Id: RCV001870892
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001293060.2:p.Gly1037Arg
CA350489351
NM_001306131.2:c.3109G>C
CA350489352
NM_001306131.2:c.3109G>A