Canonical Allele Identifier: PA2826970447
Gene: SFTPC HGNC NCBI

Linked Data

ClinVar Variation Id: 2435887
ClinVar RCV Id: RCV003136637
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001304707.1:p.Thr152Met
CA370538265
NM_001317778.2:c.455C>T