Canonical Allele Identifier: PA2828317207
Gene: FHL1 HGNC NCBI

Linked Data

ClinVar Variation Id: 469631

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356255.1:p.Asn321Asp
CA10525125
NM_001369326.1:c.961A>G