Canonical Allele Identifier: PA2829037057
Gene: SFTPC HGNC NCBI

Linked Data

ClinVar Variation Id: 3043221
ClinVar RCV Id: RCV003934033
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001372582.1:p.Gly176Glu
CA4664071
NM_001385653.1:c.527G>A