Canonical Allele Identifier: PA2825610881
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 228688
ClinVar RCV Id: RCV000213534 RCV001036640 RCV004020618
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120959.1:p.Val491Leu
CA4474354
NM_001127487.2:c.1471G>T
CA10576718
NM_001127487.2:c.1471G>C