Canonical Allele Identifier: PA210537
Gene: SFTPC HGNC NCBI

Linked Data

ClinVar Variation Id: 13208
ClinVar RCV Id: RCV000014095 RCV000731190 RCV002509156 RCV002415413
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003009.2:p.Ile73Thr
CA210536
NM_003018.4:c.218T>C