Canonical Allele Identifier: PA645490466
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_003009.2:p.Gly175Arg
CA4664070
NM_003018.4:c.523G>A
CA370538363
NM_003018.4:c.523G>C