Canonical Allele Identifier: PA2826970456
Gene: SFTPC HGNC NCBI

Linked Data

ClinVar Variation Id: 3036502
ClinVar RCV Id: RCV003921547
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001304707.1:p.Met177Val
CA4664076
NM_001317778.2:c.529A>G