Canonical Allele Identifier: PA2828318241
Gene: FHL1 HGNC NCBI

Linked Data

ClinVar Variation Id: 689589
ClinVar RCV Id: RCV000850346
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356259.1:p.Lys167Asn
CA414608676
NM_001369330.1:c.501G>C
CA414608677
NM_001369330.1:c.501G>T