Canonical Allele Identifier: PA2828041780
Gene: FGFR4 HGNC NCBI

Linked Data

ClinVar Variation Id: 1679938
ClinVar RCV Id: RCV002227947 RCV003973350
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341913.1:p.Pro136Leu
CA3575987
NM_001354984.2:c.407C>T
CA2582342973
NM_001354984.2:c.407_411delinsTCTCA