Canonical Allele Identifier: PA2826970615
Gene: SFTPC HGNC NCBI

Linked Data

ClinVar Variation Id: 362561
ClinVar RCV Id: RCV000297514 RCV000356991
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001304709.1:p.Gly169Arg
CA4664070
NM_001317780.2:c.505G>A
CA370538363
NM_001317780.2:c.505G>C