Canonical Allele Identifier: PA2826970451
Gene: SFTPC HGNC NCBI

Linked Data

ClinVar Variation Id: 362561
ClinVar RCV Id: RCV000297514 RCV000356991
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001304707.1:p.Gly169Arg
CA4664070
NM_001317778.2:c.505G>A
CA370538363
NM_001317778.2:c.505G>C